Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.13 (T)
Location

Chromosome 10:111076234 (forward strand)|View in location tab

Co-located variant

dbSNP rs1800763 (G/T)

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.111076234G>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad

About this variant

Variant displays