Variant Detail

RSID rs2957714
HGVS NC_000011.10:g.10357413T>C/G
Chromosome 11
Start position10357413
Stop position10357413
Associated gene(s)CAND1.11
Mutation typeTagged SNP
Reference T
Alternative C/G
Associated allele -
Associated African Allele Frequency 0.0490
Consequence Intronic
Other population frequencies linkALFA rs2957714

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs2957714 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases CAND1.11 rs2957714 positive Severe None None 0.0002951

Papers

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