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.
Asthma
CUI: C0004096
Disease: Asthma
714 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2020 2020
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
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
202 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
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
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
206 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
Leprosy
CUI: C0023343
Disease: Leprosy
75 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
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
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
477 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 0.500 2 2018 2019
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
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
256 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
188 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
203 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
113 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
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
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
191 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
246 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
229 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
182 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
861 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 0.500 2 2017 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2017 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
858 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 0.500 2 2017 2018