Variant Detail

RSID rs55986907
HGVS NC_000007.13:g.22817292C>T
Chromosome 7
Start position22817292
Stop position22817292
Associated gene(s)TOMM7, IL-6
Mutation typeTagged SNP
Reference C
Alternative A/T
Associated allele T
Associated African Allele Frequency 0.1494
Consequence Intergenic
Other population frequencies linkALFA rs55986907

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper