Variant Detail

RSID rs73060484
HGVS NC_000002.11:g.196364477A>C
Chromosome 2
Start position196364477
Stop position196364477
Associated gene(s)DNAH7, SLC39A10, LOC105376755
Mutation typeTagged SNP
Reference A
Alternative C
Associated allele C
Associated African Allele Frequency 0.1059
Consequence Intergenic
Other population frequencies linkALFA rs73060484

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper