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rs15 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:11563305 (GRCh38)
7:11602932 (GRCh37)
Canonical SPDI:: NC_000007.14:11563304:C:G,NC_000007.14:11563304:C:T
Gene:: THSD7A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.27007/2328 (ALFA)
C=0.109091/36 (HapMap)
C=0.138889/30 (Qatari)
C=0.149057/79 (SGDP_PRJ)
C=0.150168/39748 (TOPMED)
C=0.152873/979 (1000Genomes_30X)
C=0.159145/797 (1000Genomes)
C=0.181486/14055 (TOMMO)
C=0.2/8 (GENOME_DK)
C=0.214334/628 (KOREAN)
C=0.217249/398 (Korea1K)
C=0.222069/1606 (Korea4K)
C=0.225728/837 (TWINSUK)
C=0.227037/875 (ALSPAC)
C=0.231132/49 (Vietnamese)
C=0.259259/14 (Siberian)
C=0.263333/158 (NorthernSweden)
C=0.266741/1195 (Estonian)
C=0.287575/287 (GoNL)
HGVS:: NC_000007.14:g.11563305C>G, NC_000007.14:g.11563305C>T, NC_000007.13:g.11602932C>G, NC_000007.13:g.11602932C>T, NG_027670.2:g.273893G>C, NG_027670.2:g.273893G>A, NG_027670.1:g.273893G>C, NG_027670.1:g.273893G>A

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