Variant Detail

RSID rs920576
HGVS NC_000008.10:g.98147539T>C
Chromosome 8
Start position98147539
Stop position98147539
Associated gene(s)CPQ, LOC101927066
Mutation typeTagged SNP
Reference T
Alternative C/G
Associated allele C
Associated African Allele Frequency 0.3126
Consequence Intronic
Other population frequencies linkALFA rs920576

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper