Variant Detail

RSID rs7318817
HGVS NC_000013.11:g.28043571C>A/G/T
Chromosome 13
Start position28043571
Stop position28043571
Associated gene(s)FLT3
Mutation typeTagged SNP
Reference C
Alternative A/G/T
Associated allele -
Associated African Allele Frequency 0.6112
Consequence Intronic
Other population frequencies linkALFA rs7318817

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs7318817 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases FLT3 rs7318817 positive Severe None None 0.000654

Papers

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