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: rs10946398
rs10946398 		0.827 0.160 6 20660803 intron variant A/C snv 0.40
CUI: C0948379
Disease: Impaired insulin secretion
Impaired insulin secretion 		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: 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: 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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2012 2012
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: 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: rs10946398
rs10946398 		0.827 0.160 6 20660803 intron variant A/C snv 0.40
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.020 1.000 2 2011 2019
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: 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: 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: 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: rs6908425
rs6908425 		0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0263859
Disease: Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome
Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome 		Musculoskeletal Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6908425
rs6908425 		0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0949691
Disease: Spondylarthropathies
Spondylarthropathies 		Musculoskeletal Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6908425
rs6908425 		0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0029400
Disease: Osteitis
Osteitis 		Musculoskeletal Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6908425
rs6908425 		0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6908425
rs6908425 		0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2017 2017
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: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 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
dbSNP: rs9368197
rs9368197 		0.925 0.080 6 20533152 upstream gene variant G/T snv 0.23
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
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: rs9465871
rs9465871 		0.882 0.120 6 20717024 intron variant T/C snv 0.30
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2010 2010