rs1532268, MTRR

N. diseases: 12
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.030 1.000 3 2011 2018
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2008 2008
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2013 2013
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
58 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2011 2011
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2017 2017
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2013 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2008 2008
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2019 2019
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2005 2005
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2019 2019
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2019 2019