rs162036, MTRR

N. diseases: 6
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 0.010 1.000 1 2011 2011
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 0.010 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 0.010 1.000 1 2011 2011
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 0.010 1.000 1 2005 2005
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 0.010 1.000 1 2011 2011
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 0.010 1.000 1 2009 2009