Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 17:15164009 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950966 ; PhenCode IPNMDB_3 (G/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9889, 2010_April_001_182_PMP22_601097_0008

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

Variation displays