rs1801394, FASTKD3;MTRR

N. diseases: 101
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
122 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.846 13 1999 2019
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.895 19 2000 2017
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.889 18 2000 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 0.750 4 2002 2017
Malignant neoplasm of colon and/or rectum
502 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2002 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.900 10 2003 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.050 1.000 5 2003 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2003 2012
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2003 2009
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2003 2003
Squamous cell carcinoma of esophagus
329 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2003 2003
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2004 2014
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2004 2004
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2004 2004
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2005 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2005 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2005 2019
Squamous cell carcinoma of the head and neck
348 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2005 2007
Xanthomatosis, Cerebrotendinous
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
71 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2005 2005
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
58 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2006 2017
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2006 2006
Obesity
CUI: C0028754
Disease: Obesity
1111 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2007 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2007 2008
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2007 2019
Neurodevelopmental Disorders
CUI: C1535926
Disease: Neurodevelopmental Disorders
14 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2007 2007