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.
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2012 2012
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2014 2014
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2014 2014
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Avitaminosis
CUI: C0376286
Disease: Avitaminosis
2 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2015 2015
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
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2014 2014
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