Variant Detail

RSID rs1455662
HGVS NC_000004.12:g.179423719A>G
Chromosome 4
Start position179423719
Stop position179423719
Associated gene(s)LOC105377567
Mutation typeTagged SNP
Reference A
Alternative G
Associated allele G
Associated African Allele Frequency 0.4549
Consequence Intergenic
Other population frequencies linkALFA rs1455662

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper