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: rs387906942
rs387906942
0.925 0.040 2 74530433 missense variant C/G;T snv 4.3E-06; 4.3E-06
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs72470544
rs72470544
0.925 0.080 2 74530427 missense variant G/T snv 1.9E-02 1.7E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.020 1.000 2 2005 2011
dbSNP: rs387906942
rs387906942
0.925 0.040 2 74530433 missense variant C/G;T snv 4.3E-06; 4.3E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs72470544
rs72470544
0.925 0.080 2 74530427 missense variant G/T snv 1.9E-02 1.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs765943892
rs765943892
1.000 0.040 2 74530112 missense variant C/T snv 1.6E-04 7.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2014 2014