Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.39 (T)
Location

Chromosome 12:125320850 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56888601

This variation has 13 HGVS names - click the plus to show

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

Variation displays