DisGeNET - a database of gene-disease associations

Source: CTD_human

Disease: Autistic Disorder ×

Gene: SYNGAP1 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	8831
Gene Symbol:	SYNGAP1

SYNGAP1

CUI:	C0004352
Disease:	Autistic Disorder

Autistic Disorder

0.430

Biomarker

CTD_human

Functional impact of global rare copy number variation in autism spectrum disorders.

2010