rs326119, FASTKD3;MTRR

N. diseases: 2
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 0.925 0.120 5 7869970 intron variant C/A;G snv 0.020 1.000 2 2012 2015
Anencephaly
CUI: C0002902
Disease: Anencephaly
10 0.925 0.120 5 7869970 intron variant C/A;G snv 0.010 1.000 1 2015 2015