Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 12:56042167 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM101049, CM101048

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 21161, 21162

This variation has 12 HGVS names - click the plus to show

Variation displays