Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs34811474 1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs35789010 0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7531118 1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs17199964 4 101786634 intron variant G/A;C snv 5
rs10189857 1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs4130548 1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs3101336 1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs2650492 16 28322090 3 prime UTR variant G/A snv 0.20 5
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs2239647 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs12764899 1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs7599488 0.925 0.120 2 60491212 intron variant C/T snv 0.42 4
rs9388490 1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs6704768 1.000 0.040 2 232727791 intron variant G/A snv 0.54 4