Original source

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

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

Chromosome 1:67287825 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs386534435, rs58127206

HGVS name

1:g.67287825C>T

This variant has assays on 11 chips - click the plus to show

About this variant

This variant has 3682 sample genotypes, is associated with 4 phenotypes and is mentioned in 44 citations.

Variant displays