Variant Detail

RSID rs190509934
HGVS NC_000023.11:g.15602217T>C
Chromosome X
Start position15602217
Stop position15602217
Associated gene(s)ACE2
Mutation typeTagged SNP
Reference T
Alternative C
Associated allele C
Associated African Allele Frequency 0.0131
Consequence Intronic
Other population frequencies linkALFA rs190509934

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Horowitz_2_rs190509934 Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease COVID-19 positive vs COVID-19 negative or unknown ACE2 rs190509934 negative Susceptibility 0.3 0.6 0.00000000000045

Papers

Paper
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease