Original source

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

Alleles
A/C/T|Ancestral: T|Ambiguity code: H|MAF: 0.15 (A)
Location

Chromosome 3:55279372 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant has 4309 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays