Variant Detail

RSID rs5798227
HGVS NC_000012.12:g.52726317del
Chromosome 12
Start position52726316
Stop position52726317
Associated gene(s)KRT126P,LOC400036
Mutation typeTagged SNP
Reference CC
Alternative C
Associated allele C
Associated African Allele Frequency 0.8741
Consequence Intergenic
Other population frequencies linkALFA rs5798227

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
van_Blokland_rs5798227 Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility D1 KRT126P, LOC400036 rs5798227 Positive Mild 0.0 None 0.00000022

Papers

Paper
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility