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.
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
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
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2008 2018
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2015 2020
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2015 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2008 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2012 2014
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2011 2018
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2011 2013
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2017 2017
Meningioma, benign, no ICD-O subtype
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
30 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2017 2017
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
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: 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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2012 2014
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2017 2019
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