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: rs16940665
rs16940665
1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2011 2012
dbSNP: rs1876828
rs1876828
0.851 0.160 17 45834159 intron variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2011 2012
dbSNP: rs4525537
rs4525537
1.000 0.040 17 45835357 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2011 2012
dbSNP: rs878887
rs878887
1.000 0.040 17 45835216 3 prime UTR variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2011 2012
dbSNP: rs878888
rs878888
1.000 0.040 17 45835269 3 prime UTR variant A/G snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 2 2011 2012
dbSNP: rs12150390
rs12150390
1.000 0.040 17 45818862 intron variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1396862
rs1396862
1.000 0.040 17 45825631 non coding transcript exon variant G/A snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs16940668
rs16940668
1.000 0.040 17 45830600 non coding transcript exon variant G/A snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs16940674
rs16940674
1.000 0.040 17 45833141 missense variant C/T snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs16940676
rs16940676
1.000 0.040 17 45833670 intron variant G/A snv 0.14 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs16940677
rs16940677
1.000 0.040 17 45834532 intron variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs17425752
rs17425752
1.000 0.040 17 45829360 splice region variant A/C snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17763086
rs17763086
1.000 0.040 17 45828115 intron variant T/G snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1876829
rs1876829
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1876830
rs1876830
1.000 0.040 17 45833986 intron variant C/T snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1912151
rs1912151
1.000 0.040 17 45825578 splice region variant C/T snv 0.25 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2316765
rs2316765
1.000 0.040 17 45835088 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4482334
rs4482334
1.000 0.040 17 45835464 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4640231
rs4640231
1.000 0.040 17 45835420 3 prime UTR variant G/A;C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs878886
rs878886
0.925 0.080 17 45835124 3 prime UTR variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012