Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6605
Gene Symbol: SMARCE1
SMARCE1
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
Meningioma, benign, no ICD-O subtype 		0.040 Biomarker BEFREE The diagnostic value of SMARCE1 in distinguishing between CCM and other meningioma variants has not been yet established. 28474749

2018
Entrez Id: 6605
Gene Symbol: SMARCE1
SMARCE1
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
Meningioma, benign, no ICD-O subtype 		0.040 GeneticVariation BEFREE These results expand the spectrum of pathogenic variants in SMARCE1 and show that mutation screening can help to facilitate meningioma classification. 27891692

2017
Entrez Id: 6605
Gene Symbol: SMARCE1
SMARCE1
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
Meningioma, benign, no ICD-O subtype 		0.040 Biomarker BEFREE Recently, a second SWI/SNF complex subunit, SMARCE1, was identified as a cause of clear cell meningiomas, indicating a wider role for this complex in meningioma disease. 25857641

2015
Entrez Id: 6605
Gene Symbol: SMARCE1
SMARCE1
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
Meningioma, benign, no ICD-O subtype 		0.040 Biomarker BEFREE Together with the previous description of SMARCE1 mutations in spinal CCMs, our report suggests that SMARCE1 aberrations may be implicated in establishing a clear cell histology irrespective of meningioma location. 25249420

2015