Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs56790568

HGVS name

1:g.67281732A>C

This variation has assays on 6 chips - click the plus to show

About this variant

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

Variation displays