Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 5 chips - click the plus to show

About this variant

This variant has 4037 sample genotypes.

Variant displays