rs12785878, NADSYN1

N. diseases: 25
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 0.677 0.520 11 71456403 intron variant G/A;T snv 0.810 1.000 2 2010 2015
Vitamin D measurement
CUI: C0919758
Disease: Vitamin D measurement
51 0.677 0.520 11 71456403 intron variant G/A;T snv 0.700 1.000 1 2018 2018
Vitamin D3 measurement
CUI: C0523979
Disease: Vitamin D3 measurement
51 0.677 0.520 11 71456403 intron variant G/A;T snv 0.700 1.000 1 2018 2018
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.677 0.520 11 71456403 intron variant G/A;T snv 0.020 1.000 2 2012 2013
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.677 0.520 11 71456403 intron variant G/A;T snv 0.020 1.000 2 2013 2017
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2017 2017
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2012 2012
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2019 2019