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 5 chips - click the plus to show

Variation displays