Original source

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

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

Chromosome 12:132636864 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17771627, rs60275652

This variation has 6 HGVS names - click the plus to show

Variation displays