Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 12:109784378 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM091513, CM106803

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 33471, 13181

This variation has 34 HGVS names - click the plus to show

Variation displays