Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.48 (C)
Location

Chromosome 12:109787117 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58015411

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

This variation has assays on 6 chips - click the plus to show

Variation displays