Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51004
Gene Symbol: COQ6
COQ6 		0.300 SusceptibilityMutation disease ORPHANET A germline missense mutation in COQ6 is associated with susceptibility to familial schwannomatosis. 24763291 2014
Entrez Id: 8216
Gene Symbol: LZTR1
LZTR1 		0.300 SusceptibilityMutation disease ORPHANET Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. 24362817 2014
Entrez Id: 4771
Gene Symbol: NF2
NF2 		0.300 GeneticVariation disease ORPHANET Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria. 23401320 2013
Entrez Id: 6598
Gene Symbol: SMARCB1
SMARCB1 		0.300 GermlineCausalMutation disease ORPHANET Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria. 23401320 2013
Entrez Id: 4763
Gene Symbol: NF1
NF1 		0.300 Biomarker disease CTD_human ALTERED CALCIUM CURRENTS AND AXONAL GROWTH IN Nf1 HAPLOINSUFFICIENT MICE. 21949590 2010
Entrez Id: 6598
Gene Symbol: SMARCB1
SMARCB1 		0.300 GermlineCausalMutation disease ORPHANET Germline mutation of INI1/SMARCB1 in familial schwannomatosis. 17357086 2007