Original source

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


Genotyping chips

This variant has assays on 5 chips - Show

About this variant

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

Variant displays