Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10276782 1.000 0.040 7 24765621 regulatory region variant C/T snv 0.13 1
rs562020
KL
1.000 0.040 13 33017932 intron variant A/G snv 0.69 1
rs567170
KL
1.000 0.040 13 33043649 intron variant C/G snv 0.32 1
rs11781551 1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs17045031 1.000 0.040 3 66717940 intergenic variant G/A snv 0.10 1
rs747885829 1.000 0.040 1 247423957 missense variant C/T snv 2.0E-05 1.4E-05 1
rs6601530 1.000 0.040 8 10813762 intron variant G/A snv 0.61 1
rs4552883 0.925 0.040 8 139234730 regulatory region variant G/A;C snv 2
rs6918289 0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02 2
rs138227502 0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04 2
rs915014 0.925 0.040 1 11789412 missense variant T/C snv 2
rs4142986 0.925 0.040 9 99052344 intron variant C/A;G;T snv 1.1E-04; 0.75; 4.0E-06 2
rs495392
KL
1.000 0.040 13 33018055 intron variant C/A snv 0.24 2
rs769442590
LPL
0.925 0.040 8 19960927 missense variant A/C;G snv 1.6E-05 2
rs767523236
MPO
0.925 0.040 17 58279033 missense variant T/C snv 4.1E-06 7.0E-06 2
rs13447720 0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs499952 0.925 0.040 11 94449826 intron variant G/T snv 0.41 2
rs749582333 0.925 0.040 11 89340157 frameshift variant G/- delins 2
rs7177922 0.925 0.040 15 33616418 intron variant G/A snv 0.19 2
rs4901536 0.925 0.080 14 54733816 intron variant T/C snv 0.67 2
rs750996166 0.925 0.040 1 161041409 stop gained G/A snv 4.0E-06 7.0E-06 2
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs28937313 0.882 0.160 9 104822520 missense variant T/C snv 8.0E-06 3