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Select item 75971581.

rs7597158 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:37742548 (GRCh38)
2:37969691 (GRCh37)
Canonical SPDI:: NC_000002.12:37742547:G:A
Gene:: LOC107985869 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.034812/2696 (TOMMO)
A=0.053636/388 (Korea4K)
A=0.330306/1273 (ALSPAC)
A=0.332524/1233 (TWINSUK)
G=0.354545/117 (SGDP_PRJ)
A=0.397364/1990 (1000Genomes)
A=0.405372/2596 (1000Genomes_30X)
A=0.415803/61948 (GnomAD_genomes)
G=0.416667/5 (Siberian)
A=0.422966/111955 (TOPMED)
G=0.490741/106 (Qatari)
HGVS:: NC_000002.12:g.37742548G>A, NC_000002.11:g.37969691G>A

dbSNP