Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62274041 0.925 0.120 3 156717851 upstream gene variant G/A;T snv 3
rs6695978 0.882 0.120 1 3731781 intron variant G/A snv 7.3E-02 3
rs6755777 0.882 0.120 2 176178498 non coding transcript exon variant T/A;G snv 3
rs711830 0.882 0.120 2 176172583 3 prime UTR variant A/C;G;T snv 0.76 3
rs7260002 0.882 0.120 19 49042615 non coding transcript exon variant A/C;G snv 0.46 3
rs7365052 0.882 0.120 1 236786561 intergenic variant T/C snv 3
rs74917072 0.882 0.120 2 238022053 intron variant G/A;T snv 3
rs751039340 0.882 0.120 22 50625459 missense variant C/A snv 4.2E-06 3
rs7526063
MTR
0.882 0.120 1 236808698 splice region variant C/T snv 3.8E-02 5.6E-02 3
rs759920 0.882 0.120 19 10174102 intron variant A/G;T snv 3
rs7650365 0.882 0.120 3 128115160 intron variant G/A snv 0.35 3
rs7651446 0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs7727832 0.882 0.120 5 142611975 intron variant C/T snv 0.10 3
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 3
rs786203853 0.925 0.120 13 32339850 frameshift variant -/T delins 3
rs79722116 0.882 0.120 9 95107192 synonymous variant C/T snv 4.6E-04 2.0E-04 3
rs80357068 0.925 0.120 17 43094338 stop gained G/A;C;T snv 4.0E-06 3
rs80357760 0.925 0.120 17 43063941 frameshift variant AA/-;AAA delins 3
rs80357821 0.925 0.120 17 43094404 frameshift variant T/- delins 3
rs873330 0.882 0.120 13 104807897 intergenic variant A/G snv 0.31 3
rs876658297 0.925 0.120 17 35107108 frameshift variant TACA/- delins 7.0E-06 3
rs876658943 0.882 0.120 13 32332593 missense variant A/G snv 4.0E-06 3
rs879255288 0.882 0.120 17 43094789 missense variant T/C;G snv 4.0E-06 3
rs886040129 0.925 0.120 17 43104221 frameshift variant A/- del 3
rs886040914 0.925 0.120 17 43063872 splice donor variant A/C;G;T snv 3