Variant Detail

RSID rs531453964
HGVS NC_000008.10:g.98143139dup
Chromosome 8
Start position98143138
Stop position98143138
Associated gene(s)CPQ, LOC101927066
Mutation typeTagged SNP
Reference C
Alternative CA
Associated allele CA
Associated African Allele Frequency 0
Consequence Intronic
Other population frequencies linkALFA rs531453964

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Hu_rs531453964 Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data COVID-19 positive individuals CPQ, LOC101927066 rs531453964 Positive Severe 0.185 1.849 0.0000032

Papers

Paper
Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data