Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.19 (A)
Location

Chromosome 2:208121661 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61211452, rs17598964

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 transcript, has 3765 sample genotypes and is mentioned in 5 citations.

Variant displays