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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.100 0.909 11 2004 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.040 0.750 4 2007 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.040 0.750 4 2007 2017
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2014 2015
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2014 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2013 2015
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2005 2007
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2014 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2006 2007
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2014 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.020 1.000 2 2006 2007
5,10-Methylenetetrahydrofolate reductase deficiency
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
6 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2017 2017
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 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
Adenoma
CUI: C0001430
Disease: Adenoma
103 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
Adult Lymphoblastic Lymphoma
CUI: C0278721
Disease: Adult 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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1 2014 2014
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2010 2010
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2001 2001
Childhood Lymphoblastic Lymphoma
CUI: C0279525
Disease: Childhood 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
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2007 2007
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2018 2018
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2018 2018
Deformity
CUI: C0302142
Disease: Deformity
26 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2018 2018
Esophagitis
CUI: C0014868
Disease: Esophagitis
7 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
leukemia
CUI: C0023418
Disease: leukemia
144 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2001 2001