Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.36 (C)
Location

Chromosome 1:67281732 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56790568

HGVS name

1:g.67281732A>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 transcript, has 3687 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays