Variant Detail

RSID rs2080811
HGVS NC_000002.12:g.15584186G>A
Chromosome 2
Start position15584186
Stop position15584186
Associated gene(s)DDX1
Mutation typeTagged SNP
Reference G
Alternative A/T
Associated allele A
Associated African Allele Frequency 0.0311
Consequence Intergenic
Other population frequencies linkALFA rs2080811

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper