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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Chronic Kidney Insufficiency
CUI: C0403447
Disease: Chronic Kidney Insufficiency
12 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Chronic viral hepatitis
CUI: C0276623
Disease: Chronic viral hepatitis
8 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Rheumatism
CUI: C0035435
Disease: Rheumatism
19 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2005 2006
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2005 2006
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2003 2006
Generalized osteoarthritis
CUI: C1384584
Disease: Generalized osteoarthritis
10 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2006 2006
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2002 2006
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1 2006 2006
Carcinoma of Male Breast
CUI: C0238033
Disease: Carcinoma of Male Breast
38 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
HEMOCHROMATOSIS, TYPE 3
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
20 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Idiopathic osteoarthritis
CUI: C0409952
Disease: Idiopathic osteoarthritis
12 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
leukemia
CUI: C0023418
Disease: leukemia
144 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Malignant neoplasm of male breast
CUI: C0242787
Disease: Malignant neoplasm of male breast
43 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2002 2007
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2006 2007