Variant Detail

RSID rs151256885
HGVS NC_000017.10:g.8013217C>T
Chromosome 17
Start position8013217
Stop position8013217
Associated gene(s)ALOXE3
Mutation typeSNP
Reference C
Alternative G/T
Associated allele T
Associated African Allele Frequency 0.0161
Consequence Intronic
Other population frequencies linkALFA rs151256885

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper