Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.16 (A)
Location

Chromosome 12:51580707 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52826536

HGVS name

12:g.51580707C>A

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

Variation displays