Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.25 (T)

Chromosome 17:7281162 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3765 sample genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variant displays