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: rs369100678
rs369100678
0.925 0.040 15 61958608 missense variant C/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs869312809
rs869312809
0.925 0.040 15 61915631 splice donor variant A/C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs869312810
rs869312810
0.925 0.040 15 61882652 stop gained C/A snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs869312811
rs869312811
0.925 0.040 15 61947292 frameshift variant G/- delins
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs879253853
rs879253853
1.000 0.040 15 62013057 frameshift variant -/TCTG ins
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016