Variant Detail

RSID rs2176724
HGVS NC_000002.11:g.196952410G>A
Chromosome 2
Start position196952410
Stop position196952410
Associated gene(s)DNAH7, SLC39A18
Mutation typeTagged SNP
Reference G
Alternative A
Associated allele A
Associated African Allele Frequency 0.3642
Consequence Intergenic
Other population frequencies linkALFA rs2176724

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Hu_rs2176724 Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data COVID-19 positive individuals DNAH7, SLC39A10 rs2176724 Positive Severe 0.138 1.484 0.0061

Papers

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