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.
Cervical intraepithelial neoplasia grade 2
CUI: C0349459
Disease: Cervical intraepithelial neoplasia grade 2
3 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2013 2013
Stage III Colorectal Cancer
CUI: C0677949
Disease: Stage III Colorectal Cancer
3 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2011 2011
Stage III Colorectal Cancer AJCC v7
CUI: C3146250
Disease: Stage III Colorectal Cancer AJCC v7
3 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2011 2011
Cardiac Carcinoma
CUI: C1959584
Disease: Cardiac Carcinoma
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Laryngeal cleft
CUI: C1840311
Disease: Laryngeal cleft
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2012 2012
obsolete Combined hyperlipidemia
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Primary central nervous system lymphoma
CUI: C0280803
Disease: 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
Primary Malignant Liver Neoplasm
CUI: C0024620
Disease: Primary Malignant Liver Neoplasm
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2012 2012
5,10-Methylenetetrahydrofolate reductase deficiency
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
6 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2011 2011
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 0.500 2 2015 2015
Early childhood caries
CUI: C3714731
Disease: Early childhood caries
8 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2017 2017
Vitamin B 12 Deficiency
CUI: C0042847
Disease: Vitamin B 12 Deficiency
11 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2004 2017
Neurodevelopmental Disorders
CUI: C1535926
Disease: Neurodevelopmental Disorders
14 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
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
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2013 2013
Turner Syndrome
CUI: C0041408
Disease: Turner Syndrome
21 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2015 2015
Inattention
CUI: C0424101
Disease: Inattention
22 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2017 2017
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2013 2013
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2006 2013
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2015 2015
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2015 2015
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
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
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 1.000 3 2002 2017
Varicosity
CUI: C0042345
Disease: Varicosity
51 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2016 2016