Variant Detail

RSID rs34039247
HGVS NC_000009.11:g.136127956A>C
Chromosome 9
Start position133252569
Stop position133252569
Associated gene(s)ABO
Mutation typeTagged SNP
Reference A
Alternative C/T
Associated allele C
Associated African Allele Frequency 0.1253
Consequence 3 Prime UTR Variant
Other population frequencies linkALFA rs34039247

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Jelinek_rs34039247 Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation Critical vs non-critical (O blood group) ABO rs34039247 negative Critical None None 0.004

Papers

Paper
Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation