Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10937405 0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs112290073 0.882 0.080 5 1285917 intron variant G/A snv 7.8E-03 4
rs125555 0.882 0.080 18 50273809 missense variant G/A;C snv 3.6E-05; 0.19 4
rs1347093 0.882 0.080 2 56019205 intron variant G/T snv 0.21 4
rs138895564 0.882 0.080 5 1271959 intron variant C/T snv 5.1E-03 4
rs1397529 0.882 0.080 4 143471009 3 prime UTR variant A/C;T snv 4
rs139852726 0.882 0.080 5 1462734 3 prime UTR variant G/A;C snv 4
rs146795390 0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 8
rs199905033 0.882 0.080 5 55964205 missense variant G/C snv 4
rs2564978 0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267 0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs6495309 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10
rs12203582 0.827 0.120 6 52240759 intron variant G/A;T snv 7
rs2073664 0.851 0.120 8 42374268 synonymous variant G/A snv 0.14 0.25 5
rs2279574 0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs397517108 0.790 0.120 7 55181312 missense variant GC/TT mnv 9
rs61748181 0.827 0.120 5 1294051 missense variant C/T snv 2.2E-02 2.2E-02 10
rs121913465 0.763 0.160 7 55181312 missense variant G/T snv 11
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs3136038 0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36 13
rs2853677 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs372043866 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10