SNCA, synuclein alpha, 6622

N. diseases: 449; N. variants: 66
Disease: Fibrillation ×
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: rs104893877
rs104893877 		0.614 0.360 4 89828149 missense variant C/T snv
CUI: C0232197
Disease: Fibrillation
Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.070 1.000 7 2001 2018
dbSNP: rs542171324
rs542171324 		0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06
CUI: C0232197
Disease: Fibrillation
Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs752981956
rs752981956 		1.000 0.080 4 89822349 missense variant C/T snv 1.6E-05 1.4E-05
CUI: C0232197
Disease: Fibrillation
Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018