SNCB, synuclein beta, 6620

N. diseases: 60; N. variants: 4
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: rs104893936
rs104893936 		0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease 		Nervous System Diseases; Mental Disorders 0.730 1.000 3 2004 2009
dbSNP: rs104893937
rs104893937 		0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease 		Nervous System Diseases; Mental Disorders 0.730 1.000 3 2004 2009
dbSNP: rs778391533
rs778391533 		1.000 0.040 5 176626747 missense variant C/T snv 4.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2010 2010
dbSNP: rs104893936
rs104893936 		0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs104893936
rs104893936 		0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs104893936
rs104893936 		0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs104893937
rs104893937 		0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs104893937
rs104893937 		0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs104893937
rs104893937 		0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs35035889
rs35035889 		1.000 0.040 5 176623953 intron variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2007 2007