Variant Detail

RSID rs17854725
HGVS NC_000021.8:g.42845383A>G
Chromosome 21
Start position41473456
Stop position41473456
Associated gene(s)TMPRSS2
Mutation typeSNP
Reference A
Alternative G
Associated allele G
Associated African Allele Frequency 0.378
Consequence Synonymous variant
Other population frequencies linkALFA rs17854725

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper