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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.405 0.880 1 11794407 missense variant T/G snv 0.060 0.833 6 2007 2019
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.405 0.880 1 11794407 missense variant T/G snv 0.060 0.833 6 2005 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.800 5 2006 2013
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2008 2018
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 1999 2012
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.800 5 2012 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.800 5 2006 2019
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2011 2017
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2004 2017
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2008 2018
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2012 2017
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2011 2017
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.600 5 2005 2020
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2003 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.800 5 2003 2019
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.600 5 2013 2016
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.405 0.880 1 11794407 missense variant T/G snv 0.050 0.600 5 2005 2020
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.405 0.880 1 11794407 missense variant T/G snv 0.050 1.000 5 2009 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.405 0.880 1 11794407 missense variant T/G snv 0.040 1.000 4 2003 2007
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.405 0.880 1 11794407 missense variant T/G snv 0.040 1.000 4 2004 2017
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.405 0.880 1 11794407 missense variant T/G snv 0.040 0.250 4 2010 2015
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.405 0.880 1 11794407 missense variant T/G snv 0.040 1.000 4 2004 2017
Homocysteinemia
CUI: C3495426
Disease: Homocysteinemia
6 0.405 0.880 1 11794407 missense variant T/G snv 0.040 1.000 4 2007 2012
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.405 0.880 1 11794407 missense variant T/G snv 0.040 0.250 4 2010 2015
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.405 0.880 1 11794407 missense variant T/G snv 0.040 1.000 4 2008 2016