Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.40 (C)
Location

Chromosome 1:67294457 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs59452856

HGVS name

1:g.67294457T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant has 3687 sample genotypes, is associated with 4 phenotypes and is mentioned in 5 citations.

Variant displays