Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.29 (C)
Location

Chromosome 12:130120384 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59253827

HGVS name

12:g.130120384T>C

This variation has assays on 6 chips - click the plus to show

Variation displays