Variant Detail

RSID rs138763430
HGVS NC_000008.10:g.37707277C>T
Chromosome 8
Start position37707277
Stop position37707277
Associated gene(s)BRF2
Mutation typeSNP
Reference C
Alternative T
Associated allele T
Associated African Allele Frequency 0.0002
Consequence Missense Variant
Other population frequencies linkALFA rs138763430

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Lu_rs138763430 Genetic risk factors for death with SARS-CoV-2 from the UK Biobank COVID Death cases vs no death BRF2 rs138763430 Positive Critical None None 0.0

Papers

Paper
Genetic risk factors for death with SARS-CoV-2 from the UK Biobank