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Select item 104019781.

rs10401978 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:50859685 (GRCh38)
19:51362941 (GRCh37)
Canonical SPDI:: NC_000019.10:50859684:G:A,NC_000019.10:50859684:G:T
Gene:: KLK3 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00014/2 (ALFA)
A=0.00297/15 (1000Genomes)
G=0.5/2 (SGDP_PRJ)
HGVS:: NC_000019.10:g.50859685G>A, NC_000019.10:g.50859685G>T, NC_000019.9:g.51362941G>A, NC_000019.9:g.51362941G>T, NG_011653.1:g.9771G>A, NG_011653.1:g.9771G>T, NM_001030047.1:c.*69G>A, NM_001030047.1:c.*69G>T

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