Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs241447 0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11
rs2229116 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs11157436 0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs10808739 0.882 8 64727703 intron variant G/A snv 0.24 6
rs11790131 0.882 0.080 9 19469848 intergenic variant G/A;T snv 6
rs143633948 0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs2442719 0.882 0.120 6 31352761 intron variant C/T snv 0.53 6
rs35467001 0.882 0.080 17 73383923 missense variant G/A snv 5.3E-02 6.3E-02 6
rs35897606 0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs73084982 0.882 0.080 20 3430406 intergenic variant G/A snv 3.5E-02 6
rs73132848 0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs79709413 0.882 0.080 13 24740488 upstream gene variant G/T snv 4.7E-02 6
rs10892324 0.925 11 119032329 upstream gene variant T/A;G snv 5
rs11231017 0.925 11 62293877 downstream gene variant G/A snv 0.29 5
rs11649112 0.925 16 13267554 intron variant G/A snv 0.22 5
rs12460243 0.925 19 8066356 intron variant G/A snv 0.14 5
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5
rs16933829 0.925 11 17094129 intron variant T/C snv 6.2E-02 5
rs17038463 0.925 3 1383484 intron variant T/C;G snv 5
rs17151904 0.925 7 25568789 TF binding site variant G/A;C snv 5