Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)
Location

Chromosome 17:34355487 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

17:g.34355487G>A

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 6090 sample genotypes.

Variant displays