Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1036095 1.000 0.040 3 30620836 intron variant C/G snv 0.72 1
rs1057335 0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs1057518075 1.000 0.040 2 188995061 stop gained C/T snv 1
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10758278 1.000 0.040 9 34825306 intron variant G/A snv 0.53 1
rs10985349 1.000 0.040 9 121662964 intron variant C/T snv 0.17 1
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs12133641 0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12191786 0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs1265538677 0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs12695895 0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs12916 0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13382862 1.000 0.040 2 20682689 upstream gene variant A/G;T snv 0.59 1
rs137854485 0.925 0.160 15 48515402 missense variant G/A snv 2
rs1385526 1.000 0.040 12 57138966 intron variant G/C snv 0.26 1
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs1418184396 1.000 0.040 17 1776722 missense variant C/T snv 4.0E-06 1
rs1419338705
ELN
1.000 0.040 7 74048163 missense variant C/T snv 7.0E-06 1