Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4771
Gene Symbol: NF2
NF2 		0.500 Biomarker disease GENOMICS_ENGLAND ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
Entrez Id: 4771
Gene Symbol: NF2
NF2 		0.500 Biomarker disease GENOMICS_ENGLAND An update on age related mosaic and offspring risk in neurofibromatosis 2 (NF2). 19880713 2009
Entrez Id: 4771
Gene Symbol: NF2
NF2 		0.500 Biomarker disease CTD_human
Entrez Id: 6598
Gene Symbol: SMARCB1
SMARCB1 		0.400 Biomarker disease CTD_human Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. 24362817 2014
Entrez Id: 6598
Gene Symbol: SMARCB1
SMARCB1 		0.400 CausalMutation disease CLINVAR
Entrez Id: 8216
Gene Symbol: LZTR1
LZTR1 		0.300 Biomarker disease CTD_human Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. 24362817 2014