rs1217691063, MTHFR

N. diseases: 614
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.862 29 1998 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.964 28 2001 2018
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.926 27 2003 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.840 25 2000 2017
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.960 25 2000 2019
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 1.000 24 1999 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.826 23 2001 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.826 23 2001 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.870 23 2004 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.870 23 1996 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.826 23 2001 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.870 23 2005 2018
Methylenetetrahydrofolate reductase polymorphism
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
7 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.864 22 1999 2018
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.952 21 1997 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.895 19 2001 2015
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.944 18 2001 2017
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.941 17 2001 2017
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.941 17 2001 2017
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.941 17 1999 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.875 16 2001 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.750 16 2004 2016
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.750 16 2004 2016
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.938 16 1995 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.933 15 2004 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 1.000 14 2000 2013