Variant Detail

RSID rs9268517
HGVS NC_000006.12:g.32411963C>T
Chromosome 6
Start position32411963
Stop position32411963
Associated gene(s)BTNL2,HLA-DRA
Mutation typeSNP
Reference C
Alternative T
Associated allele T
Associated African Allele Frequency 0.0751
Consequence Downstream transcript variant
Other population frequencies linkALFA rs9268517

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper