rs1544410, VDR

N. diseases: 78
Source: BEFREE ×
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
213 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
115 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
116 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
62 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
171 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
20 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
171 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
17 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
269 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
65 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
15 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
968 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
207 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
238 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
38 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
236 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
1571 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
16 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
41 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
316 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016