Variant Detail

RSID rs34418657
HGVS NC_000003.12:g.46373293G>T
Chromosome 3
Start position46373293
Stop position46373293
Associated gene(s)CCR5
Mutation typeSNP
Reference G
Alternative A/T
Associated allele T
Associated African Allele Frequency 0
Consequence Missense Variant
Other population frequencies linkALFA rs34418657

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Cantalupo_rs34418657 Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19 Hospitalised cases with heterozygous SNP vs control CCR5 rs34418657 positive Severe None None 0.027

Papers

Paper
Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19