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: 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: 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: 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: rs17563433
rs17563433 		17 45722985 intron variant A/C snv 0.15
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17563599
rs17563599 		17 45730589 intron variant A/C snv 0.15
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs241036
rs241036 		17 45654353 non coding transcript exon variant A/C snv 0.14
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs241036
rs241036 		17 45654353 non coding transcript exon variant A/C snv 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C4284586
Disease: Perinatal depression in mother
Perinatal depression in mother 		Mental Disorders 0.010 < 0.001 1 2015 2015
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0347950
Disease: Asthma attack
Asthma attack 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs242941
rs242941 		0.790 0.200 17 45815154 intron variant A/C snv 0.62
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs439945
rs439945 		17 45649293 non coding transcript exon variant A/C snv 0.65
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17687504
rs17687504 		17 45669355 intron variant A/C;G snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs241041
rs241041 		0.925 0.120 17 45636559 non coding transcript exon variant A/C;G;T snv 0.14
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs241041
rs241041 		0.925 0.120 17 45636559 non coding transcript exon variant A/C;G;T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs241041
rs241041 		0.925 0.120 17 45636559 non coding transcript exon variant A/C;G;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: rs1724400
rs1724400 		17 45678505 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: rs385691
rs385691 		17 45648759 non coding transcript exon variant A/C;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
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: 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: rs112550936
rs112550936 		17 45638789 intron variant A/G snv 0.14
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018