Variant Detail

RSID rs2271616
HGVS NC_000003.12:g.45796521G>T
Chromosome 3
Start position45796521
Stop position45796521
Associated gene(s)SLC6A20, CCR3, LOC107986082
Mutation typeTagged SNP
Reference G
Alternative A/T
Associated allele T
Associated African Allele Frequency 0.0230
Consequence Intronic
Other population frequencies linkALFA rs2271616

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
COVID-19 HGI_rs2271616 Mapping the human genetic architecture of COVID-19 Susceptibility vs Control SLC6A20, CCR3, LOC107986082 rs2271616 Positive Mild 0.118 1.155 0.000000000000000000000000000000000179

Papers

Paper
Mapping the human genetic architecture of COVID-19