Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.26 (T)
Location

Chromosome 2:152305201 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs59050827

HGVS name

2:g.152305201A>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant has 4037 sample genotypes.

Variant displays