Variant Detail

RSID rs3787950
HGVS NC_000021.8:g.42866296T>C
Chromosome 21
Start position41494369
Stop position41494369
Associated gene(s)TMPRSS2
Mutation typeSNP
Reference T
Alternative C
Associated allele C
Associated African Allele Frequency 0.2018
Consequence Synonymous variant
Other population frequencies linkALFA rs3787950

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper