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 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
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
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2013 2017
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
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2009 2016
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.070 0.714 7 2008 2016
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
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
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2011 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2011 2018
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2011 2014
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
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2011 2013
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
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
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
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 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
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
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