rs1476413, MTHFR

N. diseases: 10
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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.700 1.000 1 2011 2011
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.020 1.000 2 2011 2016
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2012 2012
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2013 2013
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2011 2011
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2012 2012
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1 2012 2012
Mental Retardation
CUI: C0025362
Disease: Mental Retardation
98 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2011 2011
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.010 1.000 1 2012 2012