Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (T)
Location

Chromosome 12:54114819 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4445683, rs57482662

This variation has 7 HGVS names - click the plus to show

Variation displays