Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.33 (C)
Location

Chromosome 1:67747415 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56790568

HGVS name

1:g.67747415A>C

This variation has assays on 4 chips - click the plus to show

Variation displays