Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10489629 0.827 0.240 1 67222666 intron variant T/C snv 0.48 1
rs10789230 1.000 0.040 1 67264945 downstream gene variant G/C;T snv 1
rs10801047 1.000 0.040 1 191590226 intergenic variant A/T snv 0.82 1
rs10889676 0.827 0.120 1 67256884 intron variant C/A;T snv 1
rs11208994 1.000 0.040 1 67059360 regulatory region variant A/G;T snv 1
rs11209002 1.000 0.040 1 67124778 intron variant T/C snv 0.77 1
rs11209003 1.000 0.040 1 67135449 intron variant G/T snv 0.28 1
rs11209008 0.882 0.080 1 67157615 intron variant G/A;T snv 5.7E-02 1
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 1
rs11265519 1.000 0.040 1 160909123 intergenic variant C/A snv 0.60 1
rs1142287 1.000 0.040 1 155260340 synonymous variant C/T snv 0.34 0.36 1
rs11465802 1.000 0.040 1 67219915 intron variant A/C;T snv 1
rs11804284 1.000 0.040 1 67233571 intron variant T/A;C;G snv 1
rs11805303 0.827 0.240 1 67209833 intron variant C/T snv 0.30 1
rs12035082 1.000 0.040 1 172929237 intron variant T/C snv 0.52 1
rs12103 0.925 0.040 1 1312114 synonymous variant T/A;C;G snv 0.56 1
rs12567232 1.000 0.040 1 67262335 downstream gene variant G/A snv 0.27 1
rs1343151 0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs16841904 0.807 0.160 1 197732862 intron variant C/T snv 0.18 1
rs17129659 1.000 0.040 1 67113712 3 prime UTR variant C/A;T snv 8.0E-06; 6.4E-02 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs1998598 1.000 0.040 1 197758512 intron variant A/G;T snv 1
rs2064689 1.000 0.040 1 67187327 intron variant G/A snv 0.29 1
rs2488389 0.925 0.040 1 197662011 intron variant G/A snv 0.22 1