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.
Color Blindness, Blue
CUI: C0155017
Disease: Color Blindness, Blue
12 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2015 2015
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
Deformity
CUI: C0302142
Disease: Deformity
26 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2013 2013
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2013 2013
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2016 2016
Early childhood caries
CUI: C3714731
Disease: Early childhood caries
8 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
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
Glioma
CUI: C0017638
Disease: Glioma
353 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2015 2015
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
leukemia
CUI: C0023418
Disease: leukemia
144 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2014 2014
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2014 2014
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2015 2015
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
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2014 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2013 2013
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2013 2013
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2013 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2014 2014