Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.47 (T)

Chromosome 1:214968227 (forward strand) | View in location tab

Most severe consequence
Regulatory region variant
Evidence status

HGVS name


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

About this variant

This variant overlaps 1 regulatory feature and has 3173 sample genotypes.

Variant displays