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Select item 1136141171.

rs113614117 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:50869112 (GRCh38)
19:51372368 (GRCh37)
Canonical SPDI:: NC_000019.10:50869111:C:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000208/3 (ALFA)
G=0.00027/1 (TWINSUK)
G=0.000272/72 (TOPMED)
G=0.000349/49 (GnomAD)
G=0.000519/2 (ALSPAC)
G=0.001002/1 (GoNL)
HGVS:: NC_000019.10:g.50869112C>G, NC_000019.9:g.51372368C>G, NG_042791.2:g.2793C>G, NG_031984.1:g.680C>G

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