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: rs2942168
rs2942168 		0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.820 1.000 5 2011 2014
dbSNP: rs393152
rs393152 		0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.810 1.000 4 2009 2015
dbSNP: rs9303521
rs9303521 		0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs417968
rs417968 		1.000 0.040 17 45651010 non coding transcript exon variant G/A snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 5 2009 2014
dbSNP: rs7215239
rs7215239 		1.000 0.040 17 45690407 intron variant T/C snv 0.30
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 4 2011 2014
dbSNP: rs1526123
rs1526123 		1.000 0.040 17 45705974 intron variant T/C snv 0.55
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 2 2009 2012
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: rs35076622
rs35076622 		1.000 0.040 17 45779092 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
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: rs55657917
rs55657917 		17 45767194 intron variant T/G snv 0.14
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 2 2018 2018
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: rs10491143
rs10491143 		17 45695882 intron variant A/T snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs10491144
rs10491144 		17 45695758 intron variant A/C;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs10514879
rs10514879 		17 45725605 intron variant C/A;G;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1105569
rs1105569 		17 45716022 intron variant C/G;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1105571
rs1105571 		17 45715834 intron variant A/T snv 0.15
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079716
rs11079716 		17 45757507 intron variant G/A snv 0.13
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079717
rs11079717 		17 45757985 intron variant T/C snv 0.15
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079718
rs11079718 		17 45762585 intron variant A/T snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079719
rs11079719 		17 45762640 intron variant T/G snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079720
rs11079720 		17 45762650 intron variant G/A snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079721
rs11079721 		17 45762741 intron variant C/A snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11079723
rs11079723 		17 45764363 intron variant T/C snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012