Variant Detail

RSID rs35803318
HGVS NC_000023.10:g.15582209C>T
Chromosome X
Start position15564086
Stop position15564086
Associated gene(s)ACE2
Mutation typeSNP
Reference C
Alternative T
Associated allele T
Associated African Allele Frequency 0.0161
Consequence Synonymous variant
Other population frequencies linkALFA rs35803318

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper