Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.06 (C)

Chromosome 7:128954129 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs57552079, rs17338574

HGVS name


Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3613 sample genotypes, is associated with 11 phenotypes and is mentioned in 65 citations.

Variant displays