rs958546, LRRC63

N. diseases: 3
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.
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.882 0.040 13 46259582 intron variant G/C snv 0.29 0.010 1.000 1 2007 2007
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.040 13 46259582 intron variant G/C snv 0.29 0.010 1.000 1 2007 2007
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.882 0.040 13 46259582 intron variant G/C snv 0.29 0.010 1.000 1 2007 2007