Variant Detail

RSID rs199969472
HGVS NC_000009.11:g.136126498G>A
Chromosome 9
Start position133251111
Stop position133251111
Associated gene(s)ABO
Mutation typeTagged SNP
Reference G
Alternative A
Associated allele A
Associated African Allele Frequency 0.2505
Consequence 3 Prime UTR Variant
Other population frequencies linkALFA rs199969472

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Jelinek_rs199969472 Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation Critical vs non-critical (O blood group) ABO rs199969472 negative Critical None None 0.002

Papers

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