Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.02 (A)
Location

Chromosome 6:111606279 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs412224, rs58935303

HGVS name

6:g.111606279A>G

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

Variant displays