Variant Detail

RSID rs116898161
HGVS NC_000006.11:g.147538692A>G
Chromosome 6
Start position147538692
Stop position147538692
Associated gene(s)STXBP5, STXBP5-AS1
Mutation typeTagged SNP
Reference A
Alternative G
Associated allele G
Associated African Allele Frequency 0.0044
Consequence Intronic
Other population frequencies linkALFA rs116898161

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper