Original source

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

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

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

Most severe consequence
 
Regulatory region variant
Evidence status

HGVS name

1:g.214968227C>T

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