Variant Detail

RSID rs200008298
HGVS NC_000002.11:g.196602159_196602163dup
Chromosome 2
Start position196602155
Stop position196602161
Associated gene(s)SLC39A15, DNAH7, LOC107985972
Mutation typeTagged SNP
Reference A
Alternative CTATA
Associated allele CTATA
Associated African Allele Frequency 0.0202
Consequence 3 Prime UTR Variant
Other population frequencies linkALFA rs200008298

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper