Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.18 (C)

Chromosome 13:26957130 (forward strand) | View in location tab

Most severe consequence
Regulatory region variant
Evidence status


Archive dbSNP rs60996343

HGVS name


Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 4030 sample genotypes, is associated with 4 phenotypes and is mentioned in 8 citations.

Variant displays