Gene: SPTLC1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10558
Gene Symbol: SPTLC1
SPTLC1 		0.110 GeneticVariation disease BEFREE The sensorimotor neuropathy phenotype caused by the 399T-->G SPTLC1 mutation is the same as that reported by Campbell and Hoffman and, possibly, the same as that originally described by Hicks. 11479835 2001
Entrez Id: 10558
Gene Symbol: SPTLC1
SPTLC1 		0.110 CausalMutation disease CLINVAR