Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 6:3085270 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_021109

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 4 transcripts and has 3342 sample genotypes.

Variant displays