Original source

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

This variant has 2 HGVS names - Hide

17:g.47252316G>A
LRG_481:g.3475G>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3763 sample genotypes, is associated with 2 phenotypes and is mentioned in 5 citations.

Variant displays