Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 17:15239584 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930592 ; PhenCode IPNMDB_10 (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9887, 2010_April_001_180_PMP22_601097_0006

This variation has 18 HGVS names - click the plus to show

Variation displays