Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs5918 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
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 28
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41