Original source

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

A/G|Ancestral: A|Ambiguity code: R|MAF: 0.18 (G)

Chromosome 6:135105435 (forward strand)|View in location tab

Co-located variant
Most severe consequence
Upstream gene variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant overlaps 1 transcript, has 3965 sample genotypes, is associated with 7 phenotypes and is mentioned in 31 citations.

Variant displays