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: 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: 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: 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: rs110402
rs110402 		0.790 0.120 17 45802681 intron variant G/A;C snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.030 1.000 3 2013 2019
dbSNP: rs110402
rs110402 		0.790 0.120 17 45802681 intron variant G/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.030 1.000 3 2012 2016
dbSNP: rs110402
rs110402 		0.790 0.120 17 45802681 intron variant G/A;C snv
CUI: C0008060
Disease: child abuse behavior
child abuse behavior 		0.030 1.000 3 2010 2018
dbSNP: rs242939
rs242939 		0.882 0.120 17 45818213 intron variant C/T snv 0.86
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.030 1.000 3 2007 2013
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.030 1.000 3 2007 2013
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.030 1.000 3 2013 2015
dbSNP: rs7209436
rs7209436 		0.851 0.200 17 45792776 intron variant C/T snv 0.43
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.030 1.000 3 2012 2016
dbSNP: rs110402
rs110402 		0.790 0.120 17 45802681 intron variant G/A;C snv
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.020 1.000 2 2013 2019
dbSNP: rs110402
rs110402 		0.790 0.120 17 45802681 intron variant G/A;C snv
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.020 1.000 2 2011 2019
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: rs242924
rs242924 		0.882 0.080 17 45808001 intron variant G/T snv 0.44
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.020 1.000 2 2012 2016
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.020 1.000 2 2013 2015
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.020 1.000 2 2013 2015
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