Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs6589566 0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs6507931 0.882 0.080 18 49586638 intron variant C/T snv 0.52 3
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs3737787 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs3732581 0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26