This variation maps to 2 locations

Select a location:
Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (C)

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance


Uniprot VAR_065082

HGVS name


This variation has assays on 4 chips - click the plus to show

About this variant

This variant has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays