rs12638540, CMTM7

N. diseases: 1
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.
Heart failure
CUI: C0018801
Disease: Heart failure
201 1.000 0.040 3 32447042 intron variant A/G;T snv 0.800 1.000 1 2010 2010