Variant Detail

RSID rs73070529
HGVS NC_000002.11:g.196412097C>A
Chromosome 2
Start position196412097
Stop position196412097
Associated gene(s)DNAH7, SLC39A13
Mutation typeTagged SNP
Reference C
Alternative A/T
Associated allele A
Associated African Allele Frequency 0.2010
Consequence Intergenic
Other population frequencies linkALFA rs73070529

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper