rs1051266, SLC19A1

N. diseases: 41
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.
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2001 2001
leukemia
CUI: C0023418
Disease: leukemia
144 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2001 2001
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2002 2002
Congenital omphalocele
CUI: C0795690
Disease: Congenital omphalocele
13 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1 2005 2005
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2010 2010
Retinoblastoma
CUI: C0035335
Disease: Retinoblastoma
193 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2010 2010
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2011 2011
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2011 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2011 2011
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2011 2011
Squamous cell carcinoma of the head and neck
348 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2011 2011
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2012 2012
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2012 2012
Transposition of Great Vessels
CUI: C0040761
Disease: Transposition of Great Vessels
18 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2012 2012
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.070 0.857 7 2008 2013
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.070 0.857 7 2008 2013
Childhood Acute Lymphoblastic Leukemia
261 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2013 2013
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.020 1.000 2 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2014 2014
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2014 2014
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2014 2014
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2014 2014
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2015 2015
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2015 2015