DLGAP3, DLG associated protein 3, 58512

N. diseases: 18; N. variants: 6
Disease: Gilles de la Tourette syndrome ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11264126
rs11264126 		1.000 0.120 1 34876494 intron variant G/A snv 0.41
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs12141243
rs12141243 		1.000 0.120 1 34881321 intron variant T/C snv 9.7E-02
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011