Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.03 (A)
Location

Chromosome 12:11840417 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58125931, rs399828

This variation has 4 HGVS names - click the plus to show

Variation displays