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: rs16940655
rs16940655 		17 45816520 missense variant C/A;T snv 4.0E-06; 6.4E-03
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs17689471
rs17689471 		17 45815607 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
dbSNP: rs17689653
rs17689653 		17 45821597 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: rs17689824
rs17689824 		17 45827031 non coding transcript exon variant C/G;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17689882
rs17689882 		17 45829462 intron variant G/A snv 0.14
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2013 2013
dbSNP: rs17689882
rs17689882 		17 45829462 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: rs17762769
rs17762769 		17 45816037 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: rs4277389
rs4277389 		17 45818287 intron variant A/G snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4327090
rs4327090 		17 45825175 intron variant A/G snv 0.12
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4566211
rs4566211 		17 45818330 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: rs62057107
rs62057107 		17 45818666 intron variant C/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs8072451
rs8072451 		17 45816350 intron variant C/T snv 0.15
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 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: 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: rs12944712
rs12944712 		0.925 0.040 17 45793781 intron variant G/A snv 0.35
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs12944712
rs12944712 		0.925 0.040 17 45793781 intron variant G/A snv 0.35
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs12944712
rs12944712 		0.925 0.040 17 45793781 intron variant G/A snv 0.35
CUI: C0008060
Disease: child abuse behavior
child abuse behavior 		0.010 1.000 1 2014 2014
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: rs1396862
rs1396862 		1.000 0.040 17 45825631 non coding transcript exon 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: rs16940665
rs16940665 		1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		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