Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200764640 0.925 0.080 7 99666641 missense variant T/C snv 4.0E-06 2
rs34662244 0.925 0.120 6 28106103 intron variant G/A snv 5.0E-02 2
rs13054095 1.000 0.080 22 29010231 intron variant A/T snv 1.6E-02 1
rs62235753 1.000 0.080 22 28876649 intergenic variant C/T snv 1.3E-02 1
rs1190999960 0.807 0.240 11 65571690 missense variant G/A snv 9
rs3094146 1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02 1
rs8113308 0.925 0.080 19 51942133 intron variant T/C snv 0.24 2
rs3810151 0.925 0.080 19 42224684 missense variant T/C snv 0.11 7.7E-02 2
rs375066 1.000 0.080 19 43919418 intron variant T/A;C snv 1
rs9940645 0.925 0.080 16 49797677 intron variant A/G snv 0.54 2
rs10235235 0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs143072280 1.000 0.080 10 38105003 intron variant -/CTTT delins 0.40 1
rs16917302 0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs10822013 0.851 0.080 10 62492218 intron variant C/T snv 0.42 4
rs10995190 0.882 0.080 10 62518923 intron variant G/A snv 0.16 4
rs10995201 1.000 0.080 10 62540131 intron variant A/G snv 0.16 1
rs4986771 0.925 0.080 19 51965039 missense variant A/G snv 3.1E-02 2.7E-02 2
rs2278415 0.925 0.080 19 51964950 missense variant T/A snv 0.16 0.14 2
rs2278420 0.925 0.080 19 51968619 missense variant A/G snv 0.20 0.24 2
rs8109631 0.882 0.080 19 53576890 synonymous variant A/G snv 0.70 0.76 3
rs34196306 1.000 0.080 6 27457865 intron variant G/C snv 4.7E-02 1
rs704010 0.851 0.080 10 79081391 intron variant T/C snv 0.71 4
rs1250009 0.925 0.080 10 79085654 intron variant G/A;C snv 2
rs1268974 1.000 0.080 10 79092621 intron variant A/G snv 0.65 1
rs13214023 1.000 0.080 6 28364364 intron variant G/A snv 5.2E-02 1