rs7967915, LINC02463

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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 12 115875910 intron variant T/C snv 0.23 0.700 1.000 1 2013 2013