rs10304, SMTN;SELENOM

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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.925 0.120 22 31104550 3 prime UTR variant G/A snv 0.12 0.010 1.000 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.120 22 31104550 3 prime UTR variant G/A snv 0.12 0.010 1.000 1 2012 2012