Variant Detail

RSID rs75558547
HGVS NC_000001.11:g.88527468C>T
Chromosome 1
Start position88527468
Stop position88527468
Associated gene(s)PKN2-AS1
Mutation typeTagged SNP
Reference C
Alternative T
Associated allele T
Associated African Allele Frequency 0.0115
Consequence Intergenic
Other population frequencies linkALFA rs75558547

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper