rs4803455, TGFB1

N. diseases: 11
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.
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.800 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.700 1.000 1 2018 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2011 2011
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2011 2011
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2013 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2011 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2013 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2011 2011
Metastatic malignant neoplasm to brain
CUI: C0220650
Disease: Metastatic malignant neoplasm to brain
28 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1 2015 2015
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2011 2011
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.752 0.280 19 41345604 intron variant C/A snv 0.51 0.010 1.000 1 2009 2009