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: rs1994090
rs1994090
1.000 0.040 12 40034759 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.810 1.000 4 2009 2016
dbSNP: rs10877840
rs10877840
1.000 0.040 12 39959194 intron variant T/C snv 0.19
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs7304279
rs7304279
1.000 0.040 12 40072140 intron variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.710 1.000 3 2011 2014
dbSNP: rs2708453
rs2708453
1.000 0.040 12 40084850 intron variant G/T snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2012 2014
dbSNP: rs4768212
rs4768212
1.000 0.040 12 40080345 intron variant C/T snv 0.95
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2012 2014
dbSNP: rs1384236
rs1384236
1.000 0.040 12 40064582 intron variant C/T snv 0.95
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2017 2017