Variant Detail

RSID rs2923084
HGVS NC_000011.10:g.10367235A>G/T
Chromosome 11
Start position10367235
Stop position10367235
Associated gene(s)CAND1.11
Mutation typeTagged SNP
Reference A
Alternative G/T
Associated allele -
Associated African Allele Frequency 0.456
Consequence Intronic
Other population frequencies linkALFA rs2923084

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs2923084 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases CAND1.11 rs2923084 positive Severe None None 0.0000158

Papers

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