rs1801131, MTHFR

N. diseases: 93
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.
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2005 2005
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2005 2005
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.060 0.833 6 2008 2019
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2008 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.080 0.875 8 2009 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.080 0.875 8 2009 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2010 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2010 2012
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2010 2012
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2010 2012
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 0.500 2 2010 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
Orofacial cleft
CUI: C3266076
Disease: Orofacial cleft
2 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
OROFACIAL CLEFT 1
CUI: C1861537
Disease: OROFACIAL CLEFT 1
11 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
OTOFACIOCERVICAL SYNDROME 1
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
10 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
Primary central nervous system lymphoma
CUI: C0280803
Disease: Primary central nervous system lymphoma
4 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.700 1.000 1 2011 2011
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Cognitive changes
CUI: C1392786
Disease: Cognitive changes
15 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011