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.
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
15 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2014 2014
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
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
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
20 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
Metastatic melanoma
CUI: C0278883
Disease: Metastatic melanoma
22 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
25 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2015 2018
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
Primary sclerosing cholangitis
CUI: C0566602
Disease: Primary sclerosing cholangitis
26 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
27 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
33 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
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
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
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
58 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
63 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
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
Arthritis
CUI: C0003864
Disease: Arthritis
66 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
68 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2016 2019