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: rs876661321
rs876661321 		3 186841714 upstream gene variant G/T snv
CUI: C2675517
Disease: ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		0.700 0
dbSNP: rs121917815
rs121917815 		0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05
CUI: C2675517
Disease: ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		0.700 1.000 1 2000 2000
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
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 2002 2002
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs920859222
rs920859222 		1.000 0.080 3 186853158 missense variant G/A snv 1.4E-05
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2002 2002
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.020 1.000 2 2003 2003
dbSNP: rs121917815
rs121917815 		0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.710 1.000 1 2003 2003
dbSNP: rs199646033
rs199646033 		0.925 0.120 3 186854219 stop gained G/A;T snv 4.4E-05; 4.0E-06
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2003 2003
dbSNP: rs199646033
rs199646033 		0.925 0.120 3 186854219 stop gained G/A;T snv 4.4E-05; 4.0E-06
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2003 2003
dbSNP: rs199646033
rs199646033 		0.925 0.120 3 186854219 stop gained G/A;T snv 4.4E-05; 4.0E-06
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2003 2003
dbSNP: rs62625753
rs62625753 		0.925 0.120 3 186854237 missense variant G/A snv 3.0E-03 2.9E-03
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2003 2003
dbSNP: rs62625753
rs62625753 		0.925 0.120 3 186854237 missense variant G/A snv 3.0E-03 2.9E-03
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2003 2003
dbSNP: rs62625753
rs62625753 		0.925 0.120 3 186854237 missense variant G/A snv 3.0E-03 2.9E-03
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2003 2003
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.030 1.000 3 2002 2004
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs182052
rs182052 		0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs182052
rs182052 		0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C1399793
Disease: skin fold (abnormality)
skin fold (abnormality) 		0.010 1.000 1 2006 2006
dbSNP: rs2241766
rs2241766 		0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C1399793
Disease: skin fold (abnormality)
skin fold (abnormality) 		0.010 1.000 1 2006 2006