Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (C)

Chromosome 14:53944201 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status


Archive dbSNP rs57525489

HGVS name


This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2512 sample genotypes, is associated with 1 phenotype and is mentioned in 51 citations.

Variant displays