Variant Detail

RSID rs2874140
HGVS NC_000008.10:g.98142930A>T
Chromosome 8
Start position98142930
Stop position98142930
Associated gene(s)CPQ, LOC101927066
Mutation typeTagged SNP
Reference A
Alternative G/T
Associated allele T
Associated African Allele Frequency 0.3951
Consequence Intronic
Other population frequencies linkALFA rs2874140

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper