Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886041091
rs886041091
Entrez Id: 4915
Gene Symbol: NTRK2
NTRK2
CUI: C4693367
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58 		0.800 GeneticVariation UNIPROT
dbSNP: rs886041091
rs886041091
Entrez Id: 4915
Gene Symbol: NTRK2
NTRK2
CUI: C4693367
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58 		G 0.800 GeneticVariation CLINVAR
dbSNP: rs886041091
rs886041091
Entrez Id: 4915
Gene Symbol: NTRK2
NTRK2
CUI: C4693367
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58 		G 0.800 CausalMutation CLINVAR