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: 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: 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: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm 		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: C0035579
Disease: Rickets
Rickets 		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: 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: 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: 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: 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: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2016 2016
dbSNP: rs2282679
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0027651
Disease: Neoplasms
Neoplasms 		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: 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: 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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		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: C0025202
Disease: melanoma
melanoma 		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: 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: 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: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		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: 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: 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: C0948008
Disease: Ischemic stroke
Ischemic stroke 		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: 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: 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: C0019196
Disease: Hepatitis C
Hepatitis C 		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: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		0.010 1.000 1 2013 2013