Variant Detail

RSID rs2957702
HGVS NC_000011.10:g.10352760T>A/C/G
Chromosome 11
Start position10352760
Stop position10352760
Associated gene(s)CAND1.11
Mutation typeTagged SNP
Reference T
Alternative A/C/G
Associated allele -
Associated African Allele Frequency 0.5545
Consequence Intronic
Other population frequencies linkALFA rs2957702

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs2957702 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases CAND1.11 rs2957702 positive Severe None None 0.0006268

Papers

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