Variant Detail

RSID rs143359233
HGVS ENST00000204726.7:c.2812-1G>A
Chromosome 12
Start position132786788
Stop position132786788
Associated gene(s)GOLGA3
Mutation typeSNP
Reference C
Alternative T
Associated allele T
Associated African Allele Frequency 0.0008
Consequence Splice acceptor variant
Other population frequencies linkALFA rs143359233

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper