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: rs17716942
rs17716942 		0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.800 1.000 3 2010 2015
dbSNP: rs142647938
rs142647938 		0.882 2 162516642 intron variant C/A;T snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs142647938
rs142647938 		0.882 2 162516642 intron variant C/A;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs142647938
rs142647938 		0.882 2 162516642 intron variant C/A;T snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs142647938
rs142647938 		0.882 2 162516642 intron variant C/A;T snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs147910466
rs147910466 		1.000 0.040 2 162666466 intron variant A/T snv 1.1E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17716942
rs17716942 		0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs33998987
rs33998987 		1.000 0.040 2 162427557 intron variant T/C snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4667466
rs4667466 		1.000 0.120 2 162832637 intron variant T/C snv 0.52
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs2068330
rs2068330 		1.000 0.080 2 162380880 intron variant C/G snv 0.49
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.020 1.000 2 2008 2009
dbSNP: rs12104705
rs12104705 		0.882 0.120 2 162435107 intron variant C/T snv 0.15
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12104705
rs12104705 		0.882 0.120 2 162435107 intron variant C/T snv 0.15
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12104705
rs12104705 		0.882 0.120 2 162435107 intron variant C/T snv 0.15
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12104705
rs12104705 		0.882 0.120 2 162435107 intron variant C/T snv 0.15
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs78247304
rs78247304 		0.925 0.040 2 162446391 missense variant C/T snv 7.6E-05 6.4E-04
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs78247304
rs78247304 		0.925 0.040 2 162446391 missense variant C/T snv 7.6E-05 6.4E-04
CUI: C0302847
Disease: major affective disorder
major affective disorder 		0.010 1.000 1 2014 2014