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: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 1999 2011
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 1.000 12 2001 2016
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.070 0.714 7 2001 2016
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.070 0.714 7 2001 2016
dbSNP: rs149968577
rs149968577 		6 32181364 stop gained G/A;C snv 1.0E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2001 2001
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0003864
Disease: Arthritis
Arthritis 		Musculoskeletal Diseases 0.010 1.000 1 2002 2002
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.070 0.857 7 2003 2016
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2005 2019
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2005 2019
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.020 0.500 2 2005 2007
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.100 0.900 10 2007 2016
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.050 0.600 5 2007 2016
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.040 0.750 4 2007 2016
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.710 1.000 3 2007 2011
dbSNP: rs3134940
rs3134940 		0.925 0.200 6 32182039 intron variant T/C snv 0.13 0.14
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs754141936
rs754141936 		0.925 0.080 6 32182641 missense variant G/C snv 4.1E-06 1.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs754141936
rs754141936 		0.925 0.080 6 32182641 missense variant G/C snv 4.1E-06 1.4E-05
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2007 2007
dbSNP: rs900321363
rs900321363 		0.925 0.080 6 32183616 synonymous variant C/T snv 2.1E-05
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2007 2007
dbSNP: rs900321363
rs900321363 		0.925 0.080 6 32183616 synonymous variant C/T snv 2.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs1800624
rs1800624 		0.658 0.480 6 32184610 upstream gene variant A/G;T snv
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 2008 2010
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 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 0.020 1.000 2 2008 2012
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.020 1.000 2 2008 2014
dbSNP: rs2070600
rs2070600 		0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2008 2014