Source: ALL

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: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		0.810 1.000 2 2010 2015
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.020 1.000 2 2012 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.020 1.000 2 2013 2017
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2018 2018
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver 		0.010 1.000 1 2017 2017
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2018 2018
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2012 2012
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid 		0.010 1.000 1 2019 2019
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.010 1.000 1 2013 2013
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		0.010 1.000 1 2018 2018
dbSNP: rs12785878
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2018 2018