rs775144154, SLC19A1

N. diseases: 38
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.
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2004 2004
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1 2010 2010
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2006 2006
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2006 2006
Nephroblastoma
CUI: C0027708
Disease: Nephroblastoma
125 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2015 2015
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2013 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2015 2015
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2008 2008
Precursor cell lymphoblastic lymphoma
CUI: C0079748
Disease: Precursor cell lymphoblastic lymphoma
4 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2008 2008
Spina Bifida Occulta
CUI: C0080174
Disease: Spina Bifida Occulta
6 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2003 2003
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
46 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2011 2011
Stomatitis
CUI: C0038362
Disease: Stomatitis
22 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2014 2014
Thrombotic vascular disease
CUI: C4049573
Disease: Thrombotic vascular disease
1 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2005 2005