Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008257 0.925 0.040 4 94435177 intergenic variant G/A snv 0.63 2
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs1042779 0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 4
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494251 0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10503253 0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10744560 0.882 0.040 12 2277933 intron variant C/G;T snv 3
rs10748045 0.925 0.040 12 66422359 intron variant A/G snv 0.41 3
rs10774035 0.925 0.040 12 2259508 intron variant C/A;T snv 2
rs10774037 0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs10835210 0.882 0.040 11 27674363 intron variant C/A;G snv 4
rs10865974 0.925 0.040 3 52684264 intron variant G/C;T snv 2
rs10968749 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs10994338 0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 3
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11004733 0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs11714565 0.925 0.040 3 52572276 intron variant C/T snv 0.42 2