Variant Detail

RSID rs9804218
HGVS NC_000010.10:g.56495374G>C
Chromosome 10
Start position56495374
Stop position56495374
Associated gene(s)PCDH15
Mutation typeTagged SNP
Reference G
Alternative A/C
Associated allele C
Associated African Allele Frequency 0.1601
Consequence Intronic
Other population frequencies linkALFA rs9804218

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Hu_rs9804218 Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data COVID-19 positive individuals PCDH15 rs9804218 Positive Severe 0.357 1.373 0.0033

Papers

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