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: rs7719168
rs7719168
5 53996560 intron variant A/C snv 8.7E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs4311394
rs4311394
1.000 0.080 5 54004832 intron variant A/G snv 0.27
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2014 2018
dbSNP: rs4311394
rs4311394
1.000 0.080 5 54004832 intron variant A/G snv 0.27
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement
0.800 1.000 1 2009 2009
dbSNP: rs16882447
rs16882447
5 54207072 intron variant C/A snv 0.33
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs16882447
rs16882447
5 54207072 intron variant C/A snv 0.33
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0.700 1.000 1 2017 2017
dbSNP: rs255758
rs255758
1.000 0.120 5 54015672 intron variant C/A snv 0.71
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs35006
rs35006
1.000 0.040 5 54146895 intron variant C/G snv 0.24
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7735249
rs7735249
5 54014309 intron variant C/G snv 9.0E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2016 2016
dbSNP: rs7735249
rs7735249
5 54014309 intron variant C/G snv 9.0E-02
Creatinine measurement, serum (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs111366116
rs111366116
5 53999716 intron variant C/T snv 8.4E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 2 2017 2019
dbSNP: rs2441026
rs2441026
5 54148668 intron variant C/T snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2017 2019
dbSNP: rs111366116
rs111366116
5 53999716 intron variant C/T snv 8.4E-02
Creatinine measurement, serum (procedure)
0.700 1.000 1 2017 2017
dbSNP: rs114989019
rs114989019
5 53898797 intron variant C/T snv 8.1E-03
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs114989019
rs114989019
5 53898797 intron variant C/T snv 8.1E-03
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2441026
rs2441026
5 54148668 intron variant C/T snv 0.44
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs6450176
rs6450176
5 54002195 intron variant G/A snv 0.27
High density lipoprotein measurement
0.800 1.000 4 2010 2018
dbSNP: rs6450176
rs6450176
5 54002195 intron variant G/A snv 0.27
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
dbSNP: rs702634
rs702634
1.000 0.080 5 53975590 intron variant G/A snv 0.72
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 2 2014 2017
dbSNP: rs28499105
rs28499105
5 53978637 intron variant G/A snv 0.67
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs4865796
rs4865796
1.000 0.080 5 53976834 intron variant G/A snv 0.72
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs4865796
rs4865796
1.000 0.080 5 53976834 intron variant G/A snv 0.72
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4865796
rs4865796
1.000 0.080 5 53976834 intron variant G/A snv 0.72
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6450176
rs6450176
5 54002195 intron variant G/A snv 0.27
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs6450176
rs6450176
5 54002195 intron variant G/A snv 0.27
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement
0.800 1.000 1 2012 2012
dbSNP: rs702634
rs702634
1.000 0.080 5 53975590 intron variant G/A snv 0.72
CUI: C0001925
Disease: Albuminuria
Albuminuria
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018