Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11205303 0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs2816992 0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs545608 0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs1392817 0.925 0.040 1 66073773 intron variant A/G snv 0.51 3
rs10436911 0.925 0.040 1 189546287 intergenic variant A/G snv 8.3E-02 2
rs10489629 0.827 0.240 1 67222666 intron variant T/C snv 0.48 2
rs10493390 0.925 0.040 1 65846910 intron variant A/C snv 1.7E-02 2
rs10753165 0.925 0.040 1 177602999 intron variant T/A;G snv 2
rs10782606 0.925 0.040 1 76215537 intron variant G/A snv 0.67 2
rs10799667 0.925 0.040 1 20840000 intron variant T/C snv 2.7E-02 2
rs1086512 0.925 0.040 1 105694496 upstream gene variant G/T snv 2.0E-02 2
rs1086603 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 2
rs10907212 0.925 0.040 1 5722661 intergenic variant G/A snv 0.18 2
rs10910445 0.925 0.040 1 232421037 intron variant T/A;C snv 2
rs10915816 0.925 0.040 1 225374683 splice region variant C/T snv 0.81 0.73 2
rs10919410 0.925 0.040 1 170460651 non coding transcript exon variant T/A;G snv 2
rs10920828 0.925 0.040 1 190884663 intron variant G/A;C;T snv 2
rs11117615 0.925 0.040 1 216551790 intron variant T/C snv 9.9E-03 2
rs11119283 0.925 0.040 1 209467518 intergenic variant T/C snv 0.36 2
rs11184769 0.925 0.040 1 106136142 intergenic variant A/G snv 5.6E-02 2
rs11207881 0.925 0.040 1 61973715 intron variant T/C snv 3.9E-02 2
rs11240095 0.925 0.040 1 147032530 intron variant T/A snv 0.27 2
rs11264728 0.925 0.040 1 157431916 regulatory region variant A/G snv 0.30 2
rs1175646 0.925 0.040 1 112465599 upstream gene variant G/A;T snv 2
rs11801558 0.925 0.040 1 158369116 intergenic variant C/T snv 0.18 2