Variant Detail

RSID rs7817272
HGVS NC_000008.10:g.98140470T>C
Chromosome 8
Start position98140470
Stop position98140470
Associated gene(s)CPQ, LOC101927066
Mutation typeTagged SNP
Reference T
Alternative A/C/G
Associated allele C
Associated African Allele Frequency 0.35418
Consequence Intronic
Other population frequencies linkALFA rs7817272

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper