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.
pathergy
CUI: C0878631
Disease: pathergy
1 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
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
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
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
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
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
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
23 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2016 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
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
38 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2015 2018
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Metastatic melanoma
CUI: C0278883
Disease: Metastatic melanoma
42 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Primary sclerosing cholangitis
CUI: C0566602
Disease: Primary sclerosing cholangitis
58 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2016 2019
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
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
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2016 2019
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
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019