Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10159239 0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10846744 0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10918859 0.882 0.040 1 162199478 intron variant G/A snv 0.16 3
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs11014166 0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11057830 0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23