Variant Detail

RSID rs10091098
HGVS NC_000008.11:g.121836590G>A
Chromosome 8
Start position121836590
Stop position121836590
Associated gene(s)LINC02855, HAS2-AS1
Mutation typeTagged SNP
Reference G
Alternative A
Associated allele A
Associated African Allele Frequency 0.4314
Consequence Intergenic
Other population frequencies linkALFA rs10091098

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper