Original source

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

G/T | Ancestral: T | Ambiguity code: K | MAF: 0.07 (G)

Chromosome 6:111580250 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 6 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 14 transcripts, has 3739 sample genotypes and is mentioned in 2 citations.

Variant displays