Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 17:15239554 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930594 ; PhenCode IPNMDB_15 (G/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_178_PMP22_601097_0003, 9884

This variation has 16 HGVS names - click the plus to show

Variation displays