Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 17:15230952 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981609 ; PhenCode IPNMDB_31 (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9894, 2010_April_001_184_PMP22_601097_0013

This variation has 13 HGVS names - click the plus to show

Variation displays