rs765625943, MTHFR

N. diseases: 4
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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.882 0.200 1 11803417 missense variant G/A snv 4.3E-06 0.020 1.000 2 2016 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.882 0.200 1 11803417 missense variant G/A snv 4.3E-06 0.010 1.000 1 2016 2016
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.882 0.200 1 11803417 missense variant G/A snv 4.3E-06 0.010 1.000 1 2001 2001
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.882 0.200 1 11803417 missense variant G/A snv 4.3E-06 0.010 1.000 1 2010 2010