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.
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
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
1178 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
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
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
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
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
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
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 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
248 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
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
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
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
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
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