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: rs758117
rs758117 		1.000 0.040 12 2404143 intron variant C/T snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs7972947
rs7972947 		1.000 0.040 12 2061267 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2011 2013
dbSNP: rs1006737
rs1006737 		0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs1024582
rs1024582 		1.000 0.040 12 2293080 intron variant A/G;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs10491964
rs10491964 		12 2391265 intron variant G/A;C snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1057517711
rs1057517711 		1.000 0.080 12 2566466 missense variant G/A snv 7.0E-06
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs10744560
rs10744560 		0.882 0.040 12 2277933 intron variant C/G;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs10744560
rs10744560 		0.882 0.040 12 2277933 intron variant C/G;T snv
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs10744560
rs10744560 		0.882 0.040 12 2277933 intron variant C/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs10774035
rs10774035 		0.925 0.040 12 2259508 intron variant C/A;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs10774036
rs10774036 		1.000 0.040 12 2277782 intron variant C/T snv 0.25
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs10774037
rs10774037 		0.882 0.040 12 2311360 intron variant G/A snv 0.77
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs10774037
rs10774037 		0.882 0.040 12 2311360 intron variant G/A snv 0.77
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 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: rs11062098
rs11062098 		0.925 0.040 12 2065738 intron variant C/T snv 9.4E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11062098
rs11062098 		0.925 0.040 12 2065738 intron variant C/T snv 9.4E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs11062170
rs11062170 		1.000 0.040 12 2239678 intron variant G/C snv 0.26
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs117888112
rs117888112 		12 2257541 intron variant C/A snv 2.6E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs121912775
rs121912775 		1.000 0.080 12 2550020 missense variant G/A snv 6.7E-04 3.6E-04
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs121912776
rs121912776 		1.000 0.080 12 2115290 missense variant C/T snv
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs12315711
rs12315711 		1.000 0.040 12 2237664 intron variant T/A snv 0.36
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2011 2011
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: rs12425203
rs12425203 		12 2365495 intron variant C/T snv 0.36
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
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