Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.16 (A)
Location

Chromosome 2:219252736 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3806558

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

Variant displays