Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs7758512 1.000 6 30002812 intron variant T/G snv 0.17 4
rs2735076 1.000 0.040 6 29975713 intron variant A/G snv 0.71 2
rs115928623 1.000 0.080 6 29971371 intron variant A/T snv 1
rs2394250 1.000 0.040 6 29975879 intron variant G/T snv 0.40 1
rs2517873 1.000 0.080 6 29908215 intron variant G/A snv 0.15 1
rs2523933 6 29964515 intergenic variant G/C;T snv 1
rs5025708 6 29987422 intergenic variant G/T snv 0.92 1
rs9260734 1.000 0.120 6 29964889 intergenic variant G/A snv 0.22 1
rs9260742 6 29965772 intergenic variant T/A;G snv 1
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs199474387 0.807 0.240 6 29942870 missense variant G/C;T snv 6
rs1059536 1.000 0.080 6 29943448 missense variant A/C;G;T snv 4.1E-06; 0.17 3
rs199474357 0.925 0.120 6 29942790 missense variant T/C;G snv 2
rs1059449 1.000 0.120 6 29942921 missense variant G/A snv 6.1E-02 9.0E-02 1
rs199474526 1.000 0.080 6 29943384 missense variant C/A;G snv 1
rs6904029 0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26 4
rs4313034 0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 3
rs1128306 0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs2523961 0.925 0.120 6 29971803 non coding transcript exon variant G/A snv 0.16 2
rs9260151 1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 2
rs115559990 6 29926633 non coding transcript exon variant C/G;T snv 1
rs17882753 6 29944817 non coding transcript exon variant C/T snv 1.4E-02 1
rs3094146 1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02 1
rs400488 1.000 0.080 6 29975258 non coding transcript exon variant G/A snv 0.19 0.22 1