Variant Detail

RSID rs7327609
HGVS NC_000013.11:g.28090345C>A/G/T
Chromosome 13
Start position28090345
Stop position28090345
Associated gene(s)FLT3
Mutation typeTagged SNP
Reference C
Alternative A/G/T
Associated allele -
Associated African Allele Frequency 0.5764
Consequence Intronic
Other population frequencies linkALFA rs7327609

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs7327609 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases FLT3 rs7327609 positive Severe None None 0.0006437

Papers

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