rs2282679, GC

N. diseases: 38
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.810 1.000 2 2010 2015
Vitamin D measurement
CUI: C0919758
Disease: Vitamin D measurement
51 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.800 1.000 4 2010 2018
Vitamin D3 measurement
CUI: C0523979
Disease: Vitamin D3 measurement
51 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.800 1.000 4 2010 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.020 0.500 2 2012 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.020 0.500 2 2014 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.020 0.500 2 2014 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.020 0.500 2 2014 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.020 1.000 2 2012 2014
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2012 2012
Avitaminosis
CUI: C0376286
Disease: Avitaminosis
2 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2015 2015
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2014 2014
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2013 2013
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1 2014 2014
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2018 2018
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2015 2015
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2013 2013
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2013 2013
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2013 2013
Hyperparathyroidism
CUI: C0020502
Disease: Hyperparathyroidism
14 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2014 2014
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1 2014 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2013 2013
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2018 2018
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.010 1 2018 2018