Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs605143 0.882 0.040 13 110196387 intron variant C/T snv 0.34 3
rs12115090 0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs748954737
CRP
0.882 0.040 1 159713734 missense variant C/T snv 4.0E-06 3
rs77832441
CRP
0.882 0.040 1 159714024 missense variant G/A snv 1.4E-03 1.6E-03 3
rs189970623 0.882 0.040 19 41009368 missense variant C/A;G;T snv 3.0E-04 3
rs774695111 0.882 0.040 10 95069271 missense variant C/A snv 4.0E-06 3
rs747052005 0.882 0.040 15 45135527 synonymous variant T/C snv 1.6E-04 9.2E-04 3
rs1351855165 0.882 0.040 15 45111550 synonymous variant G/A snv 3
rs6020
F5
0.882 0.040 1 169549874 missense variant C/T snv 0.11 0.12 3
rs12344245 0.882 0.040 9 69340801 intron variant A/G snv 0.12 3
rs12040273 0.882 0.040 1 230063651 intron variant C/T snv 0.28 3
rs16941382 0.882 0.040 17 46966142 intron variant T/C snv 0.15 3
rs3045215 0.882 0.040 1 234605171 3 prime UTR variant -/GTTACAATA;GTTATAATA delins 3
rs1433748662 0.882 0.040 2 8791221 missense variant T/C snv 3
rs72658855 0.882 0.040 19 11100245 missense variant C/G;T snv 2.3E-03 9.4E-03 3
rs1051339 0.882 0.040 10 89247582 missense variant C/T snv 9.5E-02 0.13 3
rs774232279 0.882 0.040 15 58548572 missense variant G/A;T snv 3
rs2267788 0.882 0.040 16 9794742 intron variant C/T snv 3
rs772132247
LPL
0.882 0.040 8 19959292 missense variant G/A snv 5.2E-05 7.0E-06 3
rs731384 0.882 0.040 11 57640909 intron variant G/A snv 0.22 3
rs321159 0.882 0.040 17 32628611 intron variant A/G;T snv 3
rs2254638 0.882 0.040 21 28883961 intron variant A/C;G snv 3
rs10159239 0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs10918859 0.882 0.040 1 162199478 intron variant G/A snv 0.16 3
rs145297799 0.882 0.040 7 44539181 stop gained G/A snv 9.1E-05 9.8E-05 3