Gene: SCNM1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79005
Gene Symbol: SCNM1
SCNM1 		0.010 Biomarker phenotype BEFREE This new model suggests that SCN8A on chromosome 12q13 and SCNM1 on chromosome 1p21-1q21 may contribute to human inherited dystonia. 9949206 1999