Variant Detail

RSID rs183712207
HGVS NC_000002.11:g.196611282G>A
Chromosome 2
Start position196611282
Stop position196611282
Associated gene(s)DNAH7, SLC39A16, LOC107985972
Mutation typeTagged SNP
Reference G
Alternative A
Associated allele A
Associated African Allele Frequency 0.0045
Consequence Intronic
Other population frequencies linkALFA rs183712207

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper