Original source

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

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