rs1801394, FASTKD3;MTRR

N. diseases: 60
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.
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
49 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.080 1.000 8 1999 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.050 0.800 5 2003 2015
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
15 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.050 0.800 5 2000 2010
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.040 1.000 4 2008 2012
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.040 1.000 4 2008 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.030 1.000 3 2003 2006
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2006 2007
Childhood Acute Lymphoblastic Leukemia
97 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2007 2011
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2011 2013
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2002 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2002 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2003 2005
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
252 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2008 2009
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
409 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2006 2007
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
341 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2013 2015
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
135 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2011 2013
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 0.500 2 2007 2008
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
400 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2006 2007
Squamous cell carcinoma of the head and neck
288 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 0.500 2 2005 2007
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
364 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.020 1.000 2 2013 2015
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
26 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.010 1.000 1 2013 2013
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
99 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.010 1.000 1 2015 2015
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
9 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.010 1.000 1 2004 2004
adult meningioma
CUI: C0278877
Disease: adult meningioma
1 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.010 1.000 1 2014 2014
Avitaminosis
CUI: C0376286
Disease: Avitaminosis
1 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.010 1.000 1 2008 2008