Gene: SAMD12 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 401474
Gene Symbol: SAMD12
SAMD12 		0.120 GeneticVariation phenotype BEFREE To identify the cause of familial cortical myoclonic tremor with epilepsy pedigrees without (TTTCA)<sub>n</sub> insertions in SAMD12, TNRC6A, and RAPGEF2. 31483537 2019
Entrez Id: 401474
Gene Symbol: SAMD12
SAMD12 		0.120 GeneticVariation phenotype BEFREE Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1. 29939203 2018
Entrez Id: 401474
Gene Symbol: SAMD12
SAMD12 		0.120 Biomarker phenotype HPO