Source: BEFREE ×
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: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.966 21 2007 2019
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.958 15 2007 2019
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.890 0.889 9 2009 2019
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.060 1.000 6 2011 2017
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.060 1.000 6 2011 2017
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.030 1.000 3 2009 2018
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2011 2016
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.020 1.000 2 2011 2016
dbSNP: rs6938256
rs6938256
6 20887723 intron variant G/A;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs77152992
rs77152992
0.925 0.120 6 21065218 missense variant C/A;G;T snv 8.2E-06; 6.4E-02
CUI: C0013595
Disease: Eczema
Eczema
Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs77152992
rs77152992
0.925 0.120 6 21065218 missense variant C/A;G;T snv 8.2E-06; 6.4E-02
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C0362046
Disease: Prediabetes syndrome
Prediabetes syndrome
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C0948379
Disease: Impaired insulin secretion
Impaired insulin secretion
0.010 1.000 1 2008 2008
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2012 2012
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs981042
rs981042
0.925 0.080 6 20535303 intron variant G/T snv 0.10
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs981042
rs981042
0.925 0.080 6 20535303 intron variant G/T snv 0.10
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2206734
rs2206734
0.882 0.160 6 20694653 intron variant C/T snv 0.20
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2206734
rs2206734
0.882 0.160 6 20694653 intron variant C/T snv 0.20
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9368197
rs9368197
0.925 0.080 6 20533152 upstream gene variant G/T snv 0.23
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016