Disease: Parkinson Disease, Familial, Type 1 ×
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: rs10043
rs10043 		1.000 0.040 7 56106422 5 prime UTR variant A/C;T snv 0.80; 4.0E-06
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs142444896
rs142444896 		0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs864309650
rs864309650 		0.851 0.040 7 56104344 missense variant G/A snv
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		Nervous System Diseases 0.010 1.000 1 2019 2019