Variant Detail

RSID rs1042542
HGVS NC_000017.11:g.78225347T>C
Chromosome 17
Start position78225347
Stop position78225347
Associated gene(s)BIRC5
Mutation typeTagged SNP
Reference T
Alternative C
Associated allele -
Associated African Allele Frequency 0.6139
Consequence Non coding transcript variant
Other population frequencies linkALFA rs1042542

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Upadhyai_rs1042542 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent Asymptomatic vs Severe cases BIRC5 rs1042542 positive Severe None None 0.0004409

Papers

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