rs2780103 - SNP

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Select item 27801031.

rs2780103 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:83959653 (GRCh38)
9:86574568 (GRCh37)
Canonical SPDI:: NC_000009.12:83959652:C:G,NC_000009.12:83959652:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.186262/3422 (ALFA)
T=0.246725/452 (Korea1K)
T=0.248832/959 (ALSPAC)
T=0.252813/4237 (TOMMO)
T=0.2589/960 (TWINSUK)
T=0.259821/1164 (Estonian)
T=0.268784/787 (KOREAN)
T=0.275/11 (GENOME_DK)
T=0.275/165 (NorthernSweden)
T=0.280952/59 (Vietnamese)
T=0.291148/77064 (TOPMED)
T=0.292585/292 (GoNL)
T=0.306554/580 (HapMap)
T=0.316989/1587 (1000Genomes)
T=0.347222/75 (Qatari)
C=0.387597/100 (SGDP_PRJ)
C=0.416667/10 (Siberian)
HGVS:: NC_000009.12:g.83959653C>G, NC_000009.12:g.83959653C>T, NC_000009.11:g.86574568C>G, NC_000009.11:g.86574568C>T

Select item 593414932.

rs59341493 has merged into rs2780103 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:83959653 (GRCh38)
9:86574568 (GRCh37)
Canonical SPDI:: NC_000009.12:83959652:C:G,NC_000009.12:83959652:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.186262/3422 (ALFA)
T=0.246725/452 (Korea1K)
T=0.248832/959 (ALSPAC)
T=0.252813/4237 (TOMMO)
T=0.2589/960 (TWINSUK)
T=0.259821/1164 (Estonian)
T=0.268784/787 (KOREAN)
T=0.275/11 (GENOME_DK)
T=0.275/165 (NorthernSweden)
T=0.280952/59 (Vietnamese)
T=0.291148/77064 (TOPMED)
T=0.292585/292 (GoNL)
T=0.306554/580 (HapMap)
T=0.316989/1587 (1000Genomes)
T=0.347222/75 (Qatari)
C=0.387597/100 (SGDP_PRJ)
C=0.416667/10 (Siberian)
HGVS:: NC_000009.12:g.83959653C>G, NC_000009.12:g.83959653C>T, NC_000009.11:g.86574568C>G, NC_000009.11:g.86574568C>T