Variant Detail

RSID rs74417002
HGVS NC_000002.11:g.196384505A>G
Chromosome 2
Start position196384505
Stop position196384505
Associated gene(s)DNAH7, SLC39A12
Mutation typeTagged SNP
Reference A
Alternative G
Associated allele G
Associated African Allele Frequency 0.0608
Consequence Intergenic
Other population frequencies linkALFA rs74417002

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper