Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2662411 1.000 5 10133592 upstream gene variant G/A;C snv 5
rs28508297 1.000 14 106125683 upstream gene variant G/C snv 8.8E-02 5
rs2516928 1.000 14 106587377 upstream gene variant C/T snv 7.3E-02 5
rs2157999 1.000 12 111266635 intron variant G/A snv 8.1E-02 5
rs7719972 1.000 5 117580137 intergenic variant G/A snv 8.5E-02 5
rs7130078 1.000 11 129980320 intron variant G/A snv 5.5E-02 5
rs7126904 1.000 11 130190674 missense variant G/A snv 2.2E-02 8.8E-02 5
rs78430868 1.000 11 131630365 intron variant C/A snv 5.7E-02 5
rs2801270 1.000 21 13297803 intergenic variant A/G snv 7.8E-02 5
rs2789845 1.000 9 133934793 intron variant C/T snv 0.80 5
rs28404523 1.000 17 13627527 intergenic variant G/A snv 0.23 5
rs13391004 1.000 2 136609937 intergenic variant G/A snv 9.1E-02 5
rs9285942 1.000 5 139413007 3 prime UTR variant G/A snv 6.9E-02 5
rs2070715 1.000 5 142644691 intron variant T/C;G snv 5
rs1868175 1.000 3 143686482 intron variant A/G snv 0.75 5
rs7755842 1.000 6 144158325 intron variant A/T snv 0.10 5
rs60463810 1.000 6 148588135 intergenic variant C/T snv 0.12 5
rs61733346 1.000 7 151202976 missense variant C/G snv 9.2E-02 5
rs6596833 1.000 6 1545111 intergenic variant T/C snv 1.0E-01 5
rs2800778 1.000 1 164652278 intron variant T/G snv 0.91 5
rs5993499 1.000 22 16587858 downstream gene variant C/T snv 6.8E-02 5
rs718084 1.000 6 166681163 intron variant C/T snv 0.42 5
rs552304070 1.000 1 167426238 3 prime UTR variant AAA/-;A;AA;AAAA;AAAAAAAAA delins 4.6E-02 5
rs10039039 1.000 5 170487960 intron variant C/T snv 8.9E-02 5
rs17079875 1.000 5 179974542 intron variant G/A snv 6.8E-02 5