Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.41 (G)
Location

Chromosome 2:46369294 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58613482

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 1 transcript, has 4151 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays