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: rs1063537
rs1063537
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1063537
rs1063537
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1063537
rs1063537
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02
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: rs1063537
rs1063537
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1063537
rs1063537
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
Respiratory Tract Diseases; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1063539
rs1063539
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2020 2020
dbSNP: rs1063539
rs1063539
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1063539
rs1063539
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs1063539
rs1063539
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs121917815
rs121917815
0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs12495941
rs12495941
0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12495941
rs12495941
0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs12495941
rs12495941
0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs12495941
rs12495941
0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12495941
rs12495941
0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1259867035
rs1259867035
1.000 0.040 3 186854387 stop gained C/T snv 4.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs138227502
rs138227502
0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs138227502
rs138227502
0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs138773406
rs138773406
1.000 0.080 3 186854630 missense variant C/A;T snv 2.1E-04; 8.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs1391272583
rs1391272583
0.925 0.080 3 186853177 missense variant T/A snv 4.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1391272583
rs1391272583
0.925 0.080 3 186853177 missense variant T/A snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014