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.
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
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
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
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
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
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
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
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
Osteopenia
CUI: C0029453
Disease: Osteopenia
61 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
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
Active tuberculosis
CUI: C0151332
Disease: Active tuberculosis
25 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Chlamydia Infections
CUI: C0008149
Disease: Chlamydia Infections
10 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Familial Mediterranean Fever
CUI: C0031069
Disease: Familial Mediterranean Fever
82 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016