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 6:3110932 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_041044

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 3 transcripts and has 2504 sample genotypes.

Variant displays