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.
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.070 0.714 7 2008 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2008 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2008 2017
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
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
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
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
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
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
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
Vitamin Deficiency
CUI: C1510471
Disease: Vitamin Deficiency
2 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2008 2008
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
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2009 2009
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
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
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
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
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
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
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2012 2012