rs1805087, MTR

N. diseases: 135
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.
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 0.500 2 1997 1999
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2000 2000
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2001 2001
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2001 2001
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2002 2002
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2003 2003
Malignant neoplasm of colon and/or rectum
502 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 1999 2004
Dementia
CUI: C0497327
Disease: Dementia
176 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2004 2004
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2004 2004
Primary central nervous system lymphoma
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2004 2004
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 1.000 3 2001 2005
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2005 2005
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2005 2005
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2005 2005
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2005 2005
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2005 2005
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2006 2006
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2006 2006
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2006 2006
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2006 2006
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2001 2007
Squamous cell carcinoma of the head and neck
348 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2005 2007
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
58 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007