rs7975232, VDR

N. diseases: 56
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.
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.050 0.600 5 2015 2019
Asthma
CUI: C0004096
Disease: Asthma
1536 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.040 0.750 4 2009 2020
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2009 2017
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2012 2020
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 0.333 3 2016 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2012 2020
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2009 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2008 2019
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 0.333 3 2016 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2015 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2015 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2009 2017
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2008 2019
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 1.000 2 2007 2013
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 0.500 2 2012 2019
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 1.000 2 2016 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 1.000 2 2016 2020
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 1.000 2 2019 2020
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 1.000 2 2013 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.020 0.500 2 2018 2019
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
1178 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2018 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2015 2015
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2016 2016
Arteriovenous fistula
CUI: C0003855
Disease: Arteriovenous fistula
8 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2018 2018
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2019 2019