Original source

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

Alleles
AAC/-
Location

Chromosome 2:219421412-219421414 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_DES:c.1096_1098delAAC (AAC/-)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB DES:c.1096_1098delAAC

This variation has 8 HGVS names - click the plus to show

Variation displays