Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs1029044314 0.851 0.040 6 30898095 missense variant G/A snv 4
rs10464870 0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs10852606 0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs11233250 0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs11548193 0.925 0.040 19 48799813 missense variant G/A;C snv 0.14 2
rs11554137 0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs11558961 0.925 0.040 17 44907319 3 prime UTR variant G/C;T snv 0.27; 1.2E-05 2
rs11670188 0.925 0.040 19 2014038 non coding transcript exon variant A/G snv 0.16 2
rs11860248 0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs11979158 0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs12230172 0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs12752552 0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1306185959 0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs1320938886 0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs1340827343 0.851 0.040 6 31165259 missense variant C/T snv 4
rs1346787 0.882 0.040 2 55865477 downstream gene variant C/A;G;T snv 3
rs1373481065 0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs1381537616 0.851 0.040 7 27174132 missense variant C/T snv 4
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs145929329 0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 3
rs1558650888 0.925 0.040 2 25234308 missense variant G/A snv 2
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs1801591 0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4