Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.18 (G)
Location

Chromosome 3:7796555 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs329055, rs59505890, rs332334

HGVS name

3:g.7796555G>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant has 5537 sample genotypes and is mentioned in 2 citations.

Variant displays