Variant Detail

RSID rs9427097
HGVS NC_000001.11:g.154596207T>A/G
Chromosome 1
Start position154596207
Stop position154596207
Associated gene(s)ADAR
Mutation typeTagged SNP
Reference T
Alternative A/G
Associated allele -
Associated African Allele Frequency 0.0293
Consequence Intronic
Other population frequencies linkALFA rs9427097

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs9427097 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases ADAR rs9427097 positive Severe None None 0.0003079

Papers

Paper
Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent