Variant Detail

RSID rs12649400
HGVS NC_000004.12:g.86487989C>T
Chromosome 4
Start position86487989
Stop position86487989
Associated gene(s)MAPK10
Mutation typeTagged SNP
Reference C
Alternative T
Associated allele -
Associated African Allele Frequency 0.1482
Consequence Intronic
Other population frequencies linkALFA rs12649400

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs12649400 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases MAPK10 rs12649400 positive Severe None None 0.000649

Papers

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