Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.01 (T)
Location

Chromosome 11:2162352 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.2162352A>T

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays