Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (C)
Location

Chromosome 12:51580219 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58837806

HGVS name

12:g.51580219T>C

This variation has assays on 8 chips - click the plus to show

Variation displays