Variant Detail

RSID rs17000900
HGVS NC_000021.8:g.42798030C>A
Chromosome 21
Start position41426103
Stop position41426103
Associated gene(s)MX1
Mutation typeSNP
Reference C
Alternative A/T
Associated allele A
Associated African Allele Frequency 0.0769
Consequence Intronic
Other population frequencies linkALFA rs17000900

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value
Li_rs17000900 Genome-wide association study of COVID-19 severity among the Chinese population Meta Analysis MX1 rs17000900 negative Severe None 0.73 0.005

Papers

Paper
Genome-wide association study of COVID-19 severity among the Chinese population