Variant Detail

RSID rs657152
HGVS NC_000009.11:g.136139265C>A
Chromosome 9
Start position133263862
Stop position133263862
Associated gene(s)ABO
Mutation typeTagged SNP
Reference A
Alternative C, T
Associated allele A
Associated African Allele Frequency 0.4964
Consequence Intronic
Other population frequencies linkALFA rs657152

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Ellinghaus_rs657152 Genomewide association study of severe Covid-19 with respiratory failure Meta severity vs control ABO rs657152 Positive Severe None 1.32 0.0000000495
Roberts_rs657152 AncestryDNA COVID-19 Host Genetic Study Identifies Three Novel Loci Meta Analysis ABO rs657152 Positive Severe 0.36 1.26 0.022
Li_rs657152 Genome-wide association study of COVID-19 severity among the Chinese population combined metaanalysis ABO rs657152 positive Severe None 1.27 0.0017

Papers

Paper
Genomewide association study of severe Covid-19 with respiratory failure
AncestryDNA COVID-19 Host Genetic Study Identifies Three Novel Loci
Genome-wide association study of COVID-19 severity among the Chinese population