Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.33 (A)
Location

Chromosome 17:39884510 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs60658931, rs17305854

HGVS name

17:g.39884510G>A

Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant has 4037 sample genotypes, is associated with 7 phenotypes and is mentioned in 36 citations.

Variant displays