Name: rs7759295
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs7759295

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:41168112 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.087729 (23221/264690, TOPMED)
T=0.110980 (23985/216120, ALFA)
T=0.05467 (1545/28258, 14KJPN) (+ 19 more)
T=0.05424 (909/16760, 8.3KJPN)
T=0.0701 (449/6404, 1000G_30x)
T=0.0677 (339/5008, 1000G)
T=0.0993 (445/4480, Estonian)
T=0.1217 (469/3854, ALSPAC)
T=0.1270 (471/3708, TWINSUK)
T=0.0568 (166/2922, KOREAN)
T=0.0821 (171/2084, HGDP_Stanford)
T=0.0619 (117/1890, HapMap)
T=0.0568 (104/1832, Korea1K)
T=0.137 (137/998, GoNL)
T=0.163 (98/600, NorthernSweden)
T=0.097 (21/216, Qatari)
T=0.065 (14/214, Vietnamese)
T=0.05 (4/86, Ancient Sardinia)
C=0.45 (35/78, SGDP_PRJ)
T=0.12 (5/40, GENOME_DK)
C=0.5 (2/4, Siberian)
T=0.5 (2/4, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 4 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	216120	C=0.889020	G=0.000000, T=0.110980	0.791088	0.013048	0.195863	4
European	Sub	186422	C=0.883850	G=0.000000, T=0.116150	0.781485	0.013786	0.204729	0
African	Sub	9458	C=0.9666	G=0.0000, T=0.0334	0.93487	0.001692	0.063438	1
African Others	Sub	342	C=0.991	G=0.000, T=0.009	0.982456	0.0	0.017544	0
African American	Sub	9116	C=0.9657	G=0.0000, T=0.0343	0.933085	0.001755	0.06516	1
Asian	Sub	734	C=0.948	G=0.000, T=0.052	0.899183	0.002725	0.098093	0
East Asian	Sub	590	C=0.949	G=0.000, T=0.051	0.901695	0.00339	0.094915	0
Other Asian	Sub	144	C=0.944	G=0.000, T=0.056	0.888889	0.0	0.111111	0
Latin American 1	Sub	822	C=0.944	G=0.000, T=0.056	0.890511	0.002433	0.107056	0
Latin American 2	Sub	6810	C=0.9156	G=0.0000, T=0.0844	0.839354	0.008223	0.152423	0
South Asian	Sub	5020	C=0.8785	G=0.0000, T=0.1215	0.770916	0.013944	0.215139	0
Other	Sub	6854	C=0.8910	G=0.0000, T=0.1090	0.797199	0.015174	0.187628	3

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	C=0.912271	T=0.087729
Allele Frequency Aggregator	Total	Global	216120	C=0.889020	G=0.000000, T=0.110980
Allele Frequency Aggregator	European	Sub	186422	C=0.883850	G=0.000000, T=0.116150
Allele Frequency Aggregator	African	Sub	9458	C=0.9666	G=0.0000, T=0.0334
Allele Frequency Aggregator	Other	Sub	6854	C=0.8910	G=0.0000, T=0.1090
Allele Frequency Aggregator	Latin American 2	Sub	6810	C=0.9156	G=0.0000, T=0.0844
Allele Frequency Aggregator	South Asian	Sub	5020	C=0.8785	G=0.0000, T=0.1215
Allele Frequency Aggregator	Latin American 1	Sub	822	C=0.944	G=0.000, T=0.056
Allele Frequency Aggregator	Asian	Sub	734	C=0.948	G=0.000, T=0.052
14KJPN	JAPANESE	Study-wide	28258	C=0.94533	T=0.05467
8.3KJPN	JAPANESE	Study-wide	16760	C=0.94576	T=0.05424
1000Genomes_30x	Global	Study-wide	6404	C=0.9299	T=0.0701
1000Genomes_30x	African	Sub	1786	C=0.9720	T=0.0280
1000Genomes_30x	Europe	Sub	1266	C=0.8894	T=0.1106
1000Genomes_30x	South Asian	Sub	1202	C=0.9010	T=0.0990
1000Genomes_30x	East Asian	Sub	1170	C=0.9564	T=0.0436
1000Genomes_30x	American	Sub	980	C=0.909	T=0.091
1000Genomes	Global	Study-wide	5008	C=0.9323	T=0.0677
1000Genomes	African	Sub	1322	C=0.9728	T=0.0272
1000Genomes	East Asian	Sub	1008	C=0.9573	T=0.0427
1000Genomes	Europe	Sub	1006	C=0.8946	T=0.1054
1000Genomes	South Asian	Sub	978	C=0.906	T=0.094
1000Genomes	American	Sub	694	C=0.911	T=0.089
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9007	T=0.0993
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.8783	T=0.1217
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.8730	T=0.1270
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9432	T=0.0568
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.9179	T=0.0821
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.955	T=0.045
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.879	T=0.121
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.914	T=0.086
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.863	T=0.138
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.955	T=0.045
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.968	T=0.032
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.89	T=0.11
HapMap	Global	Study-wide	1890	C=0.9381	T=0.0619
HapMap	American	Sub	770	C=0.906	T=0.094
HapMap	African	Sub	690	C=0.968	T=0.032
HapMap	Asian	Sub	254	C=0.949	T=0.051
HapMap	Europe	Sub	176	C=0.943	T=0.057
Korean Genome Project	KOREAN	Study-wide	1832	C=0.9432	T=0.0568
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.863	T=0.137
Northern Sweden	ACPOP	Study-wide	600	C=0.837	T=0.163
Qatari	Global	Study-wide	216	C=0.903	T=0.097
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.935	T=0.065
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	86	C=0.95	T=0.05
SGDP_PRJ	Global	Study-wide	78	C=0.45	T=0.55
The Danish reference pan genome	Danish	Study-wide	40	C=0.88	T=0.12
Siberian	Global	Study-wide	4	C=0.5	T=0.5

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.41168112C>G
GRCh38.p14 chr 6	NC_000006.12:g.41168112C>T
GRCh37.p13 chr 6	NC_000006.11:g.41135850C>G
GRCh37.p13 chr 6	NC_000006.11:g.41135850C>T
TREM2 RefSeqGene (LRG_631)	NG_011561.1:g.73G>C
TREM2 RefSeqGene (LRG_631)	NG_011561.1:g.73G>A

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	C=	G	T
GRCh38.p14 chr 6	NC_000006.12:g.41168112=	NC_000006.12:g.41168112C>G	NC_000006.12:g.41168112C>T
GRCh37.p13 chr 6	NC_000006.11:g.41135850=	NC_000006.11:g.41135850C>G	NC_000006.11:g.41135850C>T
TREM2 RefSeqGene (LRG_631)	NG_011561.1:g.73=	NG_011561.1:g.73G>C	NG_011561.1:g.73G>A

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

105 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11809949	Jul 11, 2003 (116)
2	PERLEGEN	ss24436364	Sep 20, 2004 (123)
3	KRIBB_YJKIM	ss65847324	Nov 30, 2006 (127)
4	ILLUMINA	ss66627357	Nov 30, 2006 (127)
5	ILLUMINA	ss67827216	Nov 30, 2006 (127)
6	ILLUMINA	ss67989056	Nov 30, 2006 (127)
7	ILLUMINA	ss70948092	May 26, 2008 (130)
8	ILLUMINA	ss71553583	May 17, 2007 (127)
9	ILLUMINA	ss75453872	Dec 07, 2007 (129)
10	ILLUMINA	ss79269017	Dec 15, 2007 (130)
11	KRIBB_YJKIM	ss84720210	Dec 15, 2007 (130)
12	ILLUMINA	ss122828427	Dec 01, 2009 (131)
13	ILLUMINA	ss154445390	Dec 01, 2009 (131)
14	ILLUMINA	ss159620251	Dec 01, 2009 (131)
15	ILLUMINA	ss160911669	Dec 01, 2009 (131)
16	ILLUMINA	ss172343159	Jul 04, 2010 (132)
17	ILLUMINA	ss174533867	Jul 04, 2010 (132)
18	1000GENOMES	ss222354739	Jul 14, 2010 (132)
19	1000GENOMES	ss233444429	Jul 14, 2010 (132)
20	1000GENOMES	ss240507437	Jul 15, 2010 (132)
21	ILLUMINA	ss244310807	Jul 04, 2010 (132)
22	BL	ss254270648	May 09, 2011 (134)
23	GMI	ss278768788	May 04, 2012 (137)
24	ILLUMINA	ss481666177	May 04, 2012 (137)
25	ILLUMINA	ss481696883	May 04, 2012 (137)
26	ILLUMINA	ss482663948	Sep 08, 2015 (146)
27	ILLUMINA	ss485627722	May 04, 2012 (137)
28	ILLUMINA	ss537510602	Sep 08, 2015 (146)
29	TISHKOFF	ss559162777	Apr 25, 2013 (138)
30	SSMP	ss653101238	Apr 25, 2013 (138)
31	ILLUMINA	ss778985156	Sep 08, 2015 (146)
32	ILLUMINA	ss783259469	Sep 08, 2015 (146)
33	ILLUMINA	ss784212933	Sep 08, 2015 (146)
34	ILLUMINA	ss825599535	Apr 01, 2015 (144)
35	ILLUMINA	ss832520363	Sep 08, 2015 (146)
36	ILLUMINA	ss833131174	Jul 13, 2019 (153)
37	ILLUMINA	ss834447351	Sep 08, 2015 (146)
38	EVA-GONL	ss982857373	Aug 21, 2014 (142)
39	JMKIDD_LAB	ss1073561776	Aug 21, 2014 (142)
40	1000GENOMES	ss1319845751	Aug 21, 2014 (142)
41	DDI	ss1430700082	Apr 01, 2015 (144)
42	EVA_GENOME_DK	ss1581644234	Apr 01, 2015 (144)
43	EVA_DECODE	ss1592392639	Apr 01, 2015 (144)
44	EVA_UK10K_ALSPAC	ss1615430526	Apr 01, 2015 (144)
45	EVA_UK10K_TWINSUK	ss1658424559	Apr 01, 2015 (144)
46	EVA_SVP	ss1712858385	Apr 01, 2015 (144)
47	ILLUMINA	ss1752636628	Sep 08, 2015 (146)
48	HAMMER_LAB	ss1804397465	Sep 08, 2015 (146)
49	WEILL_CORNELL_DGM	ss1926113903	Feb 12, 2016 (147)
50	JJLAB	ss2023695954	Sep 14, 2016 (149)
51	USC_VALOUEV	ss2151873734	Dec 20, 2016 (150)
52	HUMAN_LONGEVITY	ss2283494279	Dec 20, 2016 (150)
53	ILLUMINA	ss2634444508	Nov 08, 2017 (151)
54	GRF	ss2707471854	Nov 08, 2017 (151)
55	ILLUMINA	ss2711076791	Nov 08, 2017 (151)
56	GNOMAD	ss2838192893	Nov 08, 2017 (151)
57	SWEGEN	ss2998949640	Nov 08, 2017 (151)
58	BIOINF_KMB_FNS_UNIBA	ss3025639795	Nov 08, 2017 (151)
59	CSHL	ss3346930068	Nov 08, 2017 (151)
60	ILLUMINA	ss3625901760	Oct 12, 2018 (152)
61	ILLUMINA	ss3629532485	Oct 12, 2018 (152)
62	ILLUMINA	ss3632361625	Oct 12, 2018 (152)
63	ILLUMINA	ss3634142678	Oct 12, 2018 (152)
64	ILLUMINA	ss3635064618	Oct 12, 2018 (152)
65	ILLUMINA	ss3635823543	Oct 12, 2018 (152)
66	ILLUMINA	ss3636787699	Oct 12, 2018 (152)
67	ILLUMINA	ss3637576353	Oct 12, 2018 (152)
68	ILLUMINA	ss3638626827	Oct 12, 2018 (152)
69	ILLUMINA	ss3639314001	Oct 12, 2018 (152)
70	ILLUMINA	ss3639682673	Oct 12, 2018 (152)
71	ILLUMINA	ss3640771917	Oct 12, 2018 (152)
72	ILLUMINA	ss3643568169	Oct 12, 2018 (152)
73	EGCUT_WGS	ss3666841297	Jul 13, 2019 (153)
74	EVA_DECODE	ss3717070840	Jul 13, 2019 (153)
75	ACPOP	ss3733442168	Jul 13, 2019 (153)
76	ILLUMINA	ss3745364546	Jul 13, 2019 (153)
77	EVA	ss3764935876	Jul 13, 2019 (153)
78	ILLUMINA	ss3772858154	Jul 13, 2019 (153)
79	KHV_HUMAN_GENOMES	ss3808082928	Jul 13, 2019 (153)
80	EVA	ss3829887687	Apr 26, 2020 (154)
81	HGDP	ss3847832070	Apr 26, 2020 (154)
82	SGDP_PRJ	ss3864433995	Apr 26, 2020 (154)
83	KRGDB	ss3911231119	Apr 26, 2020 (154)
84	KOGIC	ss3958887500	Apr 26, 2020 (154)
85	EVA	ss3985219716	Apr 26, 2021 (155)
86	TOPMED	ss4700550887	Apr 26, 2021 (155)
87	TOMMO_GENOMICS	ss5177182252	Apr 26, 2021 (155)
88	EVA	ss5237397638	Apr 26, 2021 (155)
89	1000G_HIGH_COVERAGE	ss5268194894	Oct 13, 2022 (156)
90	EVA	ss5315151988	Oct 13, 2022 (156)
91	EVA	ss5365169576	Oct 13, 2022 (156)
92	HUGCELL_USP	ss5465892535	Oct 13, 2022 (156)
93	1000G_HIGH_COVERAGE	ss5553966899	Oct 13, 2022 (156)
94	SANFORD_IMAGENETICS	ss5624628136	Oct 13, 2022 (156)
95	SANFORD_IMAGENETICS	ss5640259111	Oct 13, 2022 (156)
96	TOMMO_GENOMICS	ss5715134005	Oct 13, 2022 (156)
97	EVA	ss5799687319	Oct 13, 2022 (156)
98	YY_MCH	ss5807407120	Oct 13, 2022 (156)
99	EVA	ss5842144827	Oct 13, 2022 (156)
100	EVA	ss5847294415	Oct 13, 2022 (156)
101	EVA	ss5848095323	Oct 13, 2022 (156)
102	EVA	ss5855328560	Oct 13, 2022 (156)
103	EVA	ss5883530123	Oct 13, 2022 (156)
104	EVA	ss5968754828	Oct 13, 2022 (156)
105	EVA	ss5979785259	Oct 13, 2022 (156)
106	1000Genomes	NC_000006.11 - 41135850	Oct 12, 2018 (152)
107	1000Genomes_30x	NC_000006.12 - 41168112	Oct 13, 2022 (156)
108	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 41135850	Oct 12, 2018 (152)
109	Genetic variation in the Estonian population	NC_000006.11 - 41135850	Oct 12, 2018 (152)
110	The Danish reference pan genome	NC_000006.11 - 41135850	Apr 26, 2020 (154)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 223130850 (NC_000006.12:41168111:C:G 1/140190) Row 223130851 (NC_000006.12:41168111:C:T 12627/140162)	-	Apr 26, 2021 (155)
112	gnomAD - Genomes Submission ignored due to conflicting rows: Row 223130850 (NC_000006.12:41168111:C:G 1/140190) Row 223130851 (NC_000006.12:41168111:C:T 12627/140162)	-	Apr 26, 2021 (155)
113	Genome of the Netherlands Release 5	NC_000006.11 - 41135850	Apr 26, 2020 (154)
114	HGDP-CEPH-db Supplement 1	NC_000006.10 - 41243828	Apr 26, 2020 (154)
115	HapMap	NC_000006.12 - 41168112	Apr 26, 2020 (154)
116	KOREAN population from KRGDB	NC_000006.11 - 41135850	Apr 26, 2020 (154)
117	Korean Genome Project	NC_000006.12 - 41168112	Apr 26, 2020 (154)
118	Northern Sweden	NC_000006.11 - 41135850	Jul 13, 2019 (153)
119	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 41135850	Apr 26, 2021 (155)
120	Qatari	NC_000006.11 - 41135850	Apr 26, 2020 (154)
121	SGDP_PRJ	NC_000006.11 - 41135850	Apr 26, 2020 (154)
122	Siberian	NC_000006.11 - 41135850	Apr 26, 2020 (154)
123	8.3KJPN	NC_000006.11 - 41135850	Apr 26, 2021 (155)
124	14KJPN	NC_000006.12 - 41168112	Oct 13, 2022 (156)
125	TopMed	NC_000006.12 - 41168112	Apr 26, 2021 (155)
126	UK 10K study - Twins	NC_000006.11 - 41135850	Oct 12, 2018 (152)
127	A Vietnamese Genetic Variation Database	NC_000006.11 - 41135850	Jul 13, 2019 (153)
128	ALFA	NC_000006.12 - 41168112	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs17387458	Oct 08, 2004 (123)
rs60771149	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
1730160172	NC_000006.12:41168111:C:G	NC_000006.12:41168111:C:G	(self)
ss3639314001, ss3639682673	NC_000006.9:41243827:C:T	NC_000006.12:41168111:C:T	(self)
509962, ss254270648, ss278768788, ss481666177, ss825599535, ss1592392639, ss1712858385, ss3643568169, ss3847832070	NC_000006.10:41243827:C:T	NC_000006.12:41168111:C:T	(self)
31623920, 17636088, 12579545, 7809173, 7849248, 18408513, 6727033, 445643, 8155833, 16450975, 4390088, 35151559, 17636088, 3915788, ss222354739, ss233444429, ss240507437, ss481696883, ss482663948, ss485627722, ss537510602, ss559162777, ss653101238, ss778985156, ss783259469, ss784212933, ss832520363, ss833131174, ss834447351, ss982857373, ss1073561776, ss1319845751, ss1430700082, ss1581644234, ss1615430526, ss1658424559, ss1752636628, ss1804397465, ss1926113903, ss2023695954, ss2151873734, ss2634444508, ss2707471854, ss2711076791, ss2838192893, ss2998949640, ss3346930068, ss3625901760, ss3629532485, ss3632361625, ss3634142678, ss3635064618, ss3635823543, ss3636787699, ss3637576353, ss3638626827, ss3640771917, ss3666841297, ss3733442168, ss3745364546, ss3764935876, ss3772858154, ss3829887687, ss3864433995, ss3911231119, ss3985219716, ss5177182252, ss5237397638, ss5315151988, ss5365169576, ss5624628136, ss5640259111, ss5799687319, ss5842144827, ss5847294415, ss5848095323, ss5968754828, ss5979785259	NC_000006.11:41135849:C:T	NC_000006.12:41168111:C:T	(self)
41492834, 3117523, 15265501, 48971109, 537928445, 1730160172, ss2283494279, ss3025639795, ss3717070840, ss3808082928, ss3958887500, ss4700550887, ss5268194894, ss5465892535, ss5553966899, ss5715134005, ss5807407120, ss5855328560, ss5883530123	NC_000006.12:41168111:C:T	NC_000006.12:41168111:C:T	(self)
ss11809949	NT_007592.13:31932976:C:T	NC_000006.12:41168111:C:T	(self)
ss24436364, ss65847324, ss66627357, ss67827216, ss67989056, ss70948092, ss71553583, ss75453872, ss79269017, ss84720210, ss122828427, ss154445390, ss159620251, ss160911669, ss172343159, ss174533867, ss244310807	NT_007592.15:41075849:C:T	NC_000006.12:41168111:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

4 citations for rs7759295

PMID	Title	Author	Year	Journal
19019460	No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.	Sulonen AM et al.	2009	Journal of neuroimmunology
25545807	A TREM1 variant alters the accumulation of Alzheimer-related amyloid pathology.	Replogle JM et al.	2015	Annals of neurology
26059999	No association of TREM1 rs6910730 and TREM2 rs7759295 with Alzheimer disease.	Liu G et al.	2015	Annals of neurology
31134135	Pleiotropic Meta-Analysis of Age-Related Phenotypes Addressing Evolutionary Uncertainty in Their Molecular Mechanisms.	Kulminski AM et al.	2019	Frontiers in genetics

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

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Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
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dbSNP Short Genetic Variations

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Reference SNP (rs) Report

rs7759295