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: rs141205818
rs141205818 		1.000 0.080 3 186854691 missense variant A/C snv 3.9E-04 1.8E-04
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 < 0.001 2 2010 2014
dbSNP: rs6773957
rs6773957 		1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.800 1.000 1 2009 2009
dbSNP: rs6773957
rs6773957 		1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs16861194
rs16861194 		0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.050 0.800 5 2009 2018
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
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 2013 2016
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 0.500 2 2009 2014
dbSNP: rs16861194
rs16861194 		0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs201989364
rs201989364 		0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs201989364
rs201989364 		0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs201989364
rs201989364 		0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C0685889
Disease: Splenic Hypoplasia
Splenic Hypoplasia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
Large-artery atherosclerosis (embolus/thrombosis) 		0.010 1.000 1 2017 2017
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C0342942
Disease: Generalized obesity
Generalized obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
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 2012 2012
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
dbSNP: rs2241767
rs2241767 		0.763 0.440 3 186853407 intron variant A/G snv 0.10
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs3774261
rs3774261 		0.776 0.320 3 186853770 splice region variant A/G snv 0.55
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
Large-artery atherosclerosis (embolus/thrombosis) 		0.010 1.000 1 2017 2017