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: rs1699337
rs1699337 		3 12408594 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs1899951
rs1899951 		0.851 0.160 3 12353341 intron variant C/T snv 0.26
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 2 2012 2018
dbSNP: rs2960422
rs2960422 		1.000 0.080 3 12293492 intron variant G/A snv 0.59
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs10510418
rs10510418 		1.000 0.040 3 12347064 intron variant A/C snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10510419
rs10510419 		3 12385437 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2016 2016
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1701938
Disease: Associated Pulmonary Arterial Hypertension
Associated Pulmonary Arterial Hypertension 		Respiratory Tract Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2016 2016
dbSNP: rs10865710
rs10865710 		0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs11128597
rs11128597 		1.000 0.040 3 12303137 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11128598
rs11128598 		1.000 0.040 3 12311827 intron variant T/C snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1151996
rs1151996 		1.000 0.120 3 12404308 intron variant C/A snv 0.70
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1151999
rs1151999 		1.000 0.080 3 12405654 intron variant G/T snv 0.61
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs11709077
rs11709077 		0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11709077
rs11709077 		0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs11709077
rs11709077 		0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017