Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs174594 0.776 0.160 11 61852357 intron variant C/A;T snv 13
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174549 0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 8
rs963837 0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs9895661 0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs174566 0.925 0.160 11 61824890 intron variant A/G snv 0.34 7
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 7
rs11622435 0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs77924615 1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs174554 1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs7740107 1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs3925584 1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 6