Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)

Chromosome 11:119285483 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


Uniprot VAR_057211

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3334 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays