Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 17:47252316 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

17:g.47252316G>A

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

About this variant

This variant overlaps 3 transcripts, has 3763 sample genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variant displays