Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 12:133200748 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1135607, rs3198376

This variation has 3 HGVS names - click the plus to show

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

Variation displays