Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1002922 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 1
rs10489276 1.000 0.040 1 172893799 intron variant C/T snv 0.31 1
rs10512734 1.000 0.040 5 40393503 intergenic variant A/C;G snv 0.29 1
rs10734105 1.000 0.040 10 131373856 intergenic variant G/A;C;T snv 1
rs10789230 1.000 0.040 1 67264945 downstream gene variant G/C;T snv 1
rs10801047 1.000 0.040 1 191590226 intergenic variant A/T snv 0.82 1
rs1105267 1.000 0.040 13 20365097 intergenic variant G/A snv 0.54 1
rs1109863 1.000 0.040 16 50658453 intergenic variant G/A snv 0.69 1
rs11208994 1.000 0.040 1 67059360 regulatory region variant A/G;T snv 1
rs11229030 1.000 0.040 11 57435536 regulatory region variant C/T snv 0.55 1
rs11265519 1.000 0.040 1 160909123 intergenic variant C/A snv 0.60 1
rs11679753 1.000 0.040 2 62325186 regulatory region variant A/C;G;T snv 1
rs11894081 1.000 0.040 2 5523876 intergenic variant G/T snv 0.57 1
rs1199103 1.000 0.040 10 58187470 downstream gene variant A/C;G snv 1
rs1200332 1.000 0.040 14 34897929 intergenic variant T/C snv 0.67 1
rs12035082 1.000 0.040 1 172929237 intron variant T/C snv 0.52 1
rs12422544 1.000 0.040 12 40134630 intergenic variant T/C snv 2.7E-02 1
rs12552933 1.000 0.040 9 114759302 intergenic variant C/T snv 2.9E-02 1
rs12567232 1.000 0.040 1 67262335 downstream gene variant G/A snv 0.27 1
rs12576495 1.000 0.040 11 93131841 upstream gene variant T/C snv 0.23 1
rs12663356 1.000 0.040 6 21430497 intergenic variant T/C snv 0.52 1
rs12922698 1.000 0.040 16 50815062 intergenic variant C/T snv 0.23 1
rs12985909 1.000 0.040 19 18328573 upstream gene variant C/T snv 0.51 1
rs13073817 1.000 0.040 3 18665366 intron variant G/A;C snv 1
rs13371189 1.000 0.040 18 11304692 intergenic variant A/C snv 1