Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		0.810 1.000 1 2010 2015
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 0.500 2 2014 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 0.500 2 2012 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 1.000 2 2012 2014
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.020 0.500 2 2014 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 0.500 2 2014 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2017 2017
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2018 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		0.010 1.000 1 2013 2013
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2013 2013
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.010 1.000 1 2014 2014
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 < 0.001 1 2014 2014
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 < 0.001 1 2016 2016
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 < 0.001 1 2018 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.010 1.000 1 2013 2013
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 < 0.001 1 2018 2018
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2015 2015
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2014 2014
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2014 2014
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		0.010 1.000 1 2014 2014
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C1510471
Disease: Vitamin Deficiency
Vitamin Deficiency 		0.010 1.000 1 2015 2015
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2012 2012
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.010 1.000 1 2013 2013