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: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11671664
rs11671664 		0.925 0.120 19 45669020 intron variant G/A snv 0.12
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2302382
rs2302382 		1.000 0.080 19 45669311 splice region variant C/A snv 0.18
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 2017 2017
dbSNP: rs759364715
rs759364715 		1.000 0.040 19 45672880 missense variant G/A snv 2.0E-05 2.1E-05
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs759364715
rs759364715 		1.000 0.040 19 45672880 missense variant G/A snv 2.0E-05 2.1E-05
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.810 1.000 2 2013 2019
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.710 1.000 2 2017 2018
dbSNP: rs10423928
rs10423928 		0.807 0.200 19 45679046 intron variant T/A snv 0.19
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2012 2016
dbSNP: rs11671664
rs11671664 		0.925 0.120 19 45669020 intron variant G/A snv 0.12
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 3 2012 2014
dbSNP: rs11671664
rs11671664 		0.925 0.120 19 45669020 intron variant G/A snv 0.12
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 3 2012 2014
dbSNP: rs11672660
rs11672660 		19 45676926 intron variant C/T snv 0.18 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2019
dbSNP: rs1800437
rs1800437 		0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2017 2019
dbSNP: rs11671664
rs11671664 		0.925 0.120 19 45669020 intron variant G/A snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2012 2017