Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.35 (G)
Location

Chromosome 2:210310319 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58784217, rs4353584

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 1 transcript, has 2627 sample genotypes and is associated with 2 phenotypes.

Variant displays