Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.34254259A>C

This variant has assays on 5 chips - click the plus to show

About this variant

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

Variant displays