Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.33 (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 2284 individual genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variation displays