Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.08 (-)
Location

Chromosome 12:133211246 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 10 HGVS names - click the plus to show

Variation displays