rs397507444, MTHFR

N. diseases: 306
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.
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.405 0.880 1 11794407 missense variant T/G snv 0.100 0.727 11 2004 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.405 0.880 1 11794407 missense variant T/G snv 0.100 0.900 10 2002 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.667 9 2001 2018
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 2004 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 2002 2017
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 1999 2020
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 2000 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.667 9 2001 2018
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 2004 2014
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.667 9 2001 2018
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.405 0.880 1 11794407 missense variant T/G snv 0.080 1.000 8 2005 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.405 0.880 1 11794407 missense variant T/G snv 0.080 1.000 8 2005 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.405 0.880 1 11794407 missense variant T/G snv 0.080 1.000 8 2006 2018
Malignant neoplasm of urinary bladder
316 0.405 0.880 1 11794407 missense variant T/G snv 0.080 1.000 8 2005 2013
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.405 0.880 1 11794407 missense variant T/G snv 0.080 0.750 8 2003 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.405 0.880 1 11794407 missense variant T/G snv 0.070 0.714 7 2002 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.405 0.880 1 11794407 missense variant T/G snv 0.070 0.857 7 2012 2018
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.405 0.880 1 11794407 missense variant T/G snv 0.070 1.000 7 2004 2019
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.405 0.880 1 11794407 missense variant T/G snv 0.070 0.857 7 2012 2019
Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.405 0.880 1 11794407 missense variant T/G snv 0.070 1.000 7 2004 2015
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.405 0.880 1 11794407 missense variant T/G snv 0.060 1.000 6 2007 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.405 0.880 1 11794407 missense variant T/G snv 0.060 0.833 6 2012 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.405 0.880 1 11794407 missense variant T/G snv 0.060 0.833 6 2008 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.405 0.880 1 11794407 missense variant T/G snv 0.060 1.000 6 2007 2015
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.405 0.880 1 11794407 missense variant T/G snv 0.060 0.833 6 2012 2018