rs1544410, VDR

N. diseases: 78
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2005 2018
Postsurgical menopause
CUI: C0740421
Disease: Postsurgical menopause
2 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2006 2006
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2007 2018
HIV-1 infection
CUI: C2363741
Disease: HIV-1 infection
94 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2008 2010
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2008 2008
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2008 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.070 0.714 7 2009 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.070 0.714 7 2009 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2009 2019
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2009 2009
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2011 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2011 2011
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.040 1.000 4 2012 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2012 2017
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2012 2012
Congenital contractural arachnodactyly
CUI: C0220668
Disease: Congenital contractural arachnodactyly
48 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2012 2012
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2012 2012
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 2 2013 2019
Periodontal Diseases
CUI: C0031090
Disease: Periodontal Diseases
22 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.040 1.000 4 2014 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.030 1.000 3 2014 2018
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
19 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2014 2014
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1 2014 2014
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2014 2014
Rickets
CUI: C0035579
Disease: Rickets
16 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2014 2014