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: rs2239063
rs2239063 		1.000 0.040 12 2402665 intron variant A/C snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs2239063
rs2239063 		1.000 0.040 12 2402665 intron variant A/C snv 0.23
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4765904
rs4765904 		1.000 0.040 12 2223227 intron variant A/C snv 0.36
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs2007044
rs2007044 		0.882 0.040 12 2235794 intron variant A/G snv 0.50
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.710 1.000 7 2014 2019
dbSNP: rs10848642
rs10848642 		1.000 0.040 12 2222406 non coding transcript exon variant A/G snv 0.37
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs12322010
rs12322010 		12 2542721 intron variant A/G snv 4.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12424245
rs12424245 		1.000 0.040 12 2213347 intron variant A/G snv 0.26
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs12823424
rs12823424 		1.000 0.040 12 2404946 intron variant A/G snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs186867242
rs186867242 		1.000 0.200 12 2686232 missense variant A/G snv 2.2E-04 4.9E-05
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2007044
rs2007044 		0.882 0.040 12 2235794 intron variant A/G snv 0.50
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs2007044
rs2007044 		0.882 0.040 12 2235794 intron variant A/G snv 0.50
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs2007044
rs2007044 		0.882 0.040 12 2235794 intron variant A/G snv 0.50
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs2007044
rs2007044 		0.882 0.040 12 2235794 intron variant A/G snv 0.50
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs2007044
rs2007044 		0.882 0.040 12 2235794 intron variant A/G snv 0.50
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2108635
rs2108635 		12 2050390 intron variant A/G snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2239051
rs2239051 		12 2343026 intron variant A/G snv 2.0E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2239051
rs2239051 		12 2343026 intron variant A/G snv 2.0E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2239051
rs2239051 		12 2343026 intron variant A/G snv 2.0E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2239051
rs2239051 		12 2343026 intron variant A/G snv 2.0E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4298967
rs4298967 		1.000 0.040 12 2299028 intron variant A/G snv 0.74
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs7311607
rs7311607 		12 2413815 intron variant A/G snv 0.34
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7312105
rs7312105 		12 2414189 intron variant A/G snv 0.34
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2012 2012
dbSNP: rs7312105
rs7312105 		12 2414189 intron variant A/G snv 0.34
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs882194
rs882194 		1.000 0.040 12 2241286 intron variant A/G snv 0.53
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1024582
rs1024582 		1.000 0.040 12 2293080 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.710 1.000 3 2014 2019