Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10053538 0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10754339 0.882 0.120 1 117147650 3 prime UTR variant G/A snv 0.88 0.76 3
rs10877887 0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11225395 0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11730582 0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37 10
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1256054 0.882 0.120 14 64249595 synonymous variant G/C snv 2.8E-03 9.6E-04 3
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1455751791 0.882 0.120 6 152011735 synonymous variant C/G snv 4.0E-06 3