Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 17:34254259 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays