Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)

Chromosome 22:35067169 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_032448

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3917 sample genotypes and is mentioned in 3 citations.

Variant displays