Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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