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Select item 47882291.

rs4788229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 1:121742903 (GRCh38)
1:121484701 (GRCh37)
Canonical SPDI:: NC_000001.11:121742902:T:A,NC_000001.11:121742902:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
A=0.000156/1 (1000Genomes_30X)
A=0.0002/1 (1000Genomes)
HGVS:: NC_000001.11:g.121742903T>A, NC_000001.11:g.121742903T>G, NC_000001.10:g.121484701T>A, NC_000001.10:g.121484701T>G, NG_092017.1:g.675T>A, NG_092017.1:g.675T>G, NG_098414.1:g.20T>A, NG_098414.1:g.20T>G

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