Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.03 (-)
Location

Chromosome 12:12715467 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs369210266, rs142904407

This variation has 2 HGVS names - click the plus to show

Variation displays