Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.04 (C)

Chromosome 11:72015122 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_031680

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 20 transcripts, has 2545 sample genotypes and is mentioned in 3 citations.

Variant displays