Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9973676 1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs9632885 1.000 0.040 9 22072639 intron variant G/A snv 0.56 2
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs944801 0.882 0.120 9 22051671 intron variant G/A;C snv 4
rs944799 1.000 0.040 9 22050614 intron variant A/G snv 0.50 2
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs9384331 1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs91 1.000 0.080 7 24409992 intron variant T/C snv 0.41 2
rs8181050 1.000 0.040 9 22064392 intron variant G/A;C;T snv 2
rs8134546 1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs8089491 18 31763291 upstream gene variant G/A snv 5.4E-02 1
rs7866783 1.000 0.040 9 22056360 non coding transcript exon variant A/G snv 0.71 2
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs7859727 1.000 0.080 9 22102166 intron variant C/T snv 0.57 3
rs7859362 9 22105928 intron variant T/C snv 0.64 2
rs7857345 0.925 0.080 9 22087474 non coding transcript exon variant T/A;C snv 4
rs7857118 9 22124141 intron variant A/T snv 0.64 1
rs7804216 1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs77757620 1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2