Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5888 0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131