Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7773694 0.882 0.280 6 32738557 upstream gene variant A/G snv 0.80 3
rs9268615 0.882 0.280 6 32435112 upstream gene variant G/A snv 0.38 3
rs9276162 0.882 0.280 6 32730680 downstream gene variant G/A snv 0.74 3
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs11752643 0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02 2
rs13199787 0.925 0.200 6 32737499 upstream gene variant C/T snv 0.38 2
rs1383265 0.925 0.200 6 32772111 intergenic variant T/A;C snv 2
rs154972 0.925 0.120 6 32932874 downstream gene variant A/G snv 0.35 2
rs2213573 0.925 0.200 6 32748245 downstream gene variant G/A snv 0.80 2
rs2395309 0.925 0.200 6 33058469 regulatory region variant A/G;T snv 0.28 2
rs2532932 0.925 0.160 6 30927667 downstream gene variant A/G snv 0.74 2
rs2856726 1.000 0.080 6 32698944 intergenic variant A/T snv 0.34 2
rs2858312 1.000 0.080 6 32699453 intergenic variant G/C snv 0.32 2
rs3094137 0.925 0.120 6 30233096 downstream gene variant A/G;T snv 2
rs3104404 0.925 0.160 6 32714397 upstream gene variant C/A snv 0.24 2
rs422544 0.925 0.120 6 33058333 regulatory region variant A/C snv 0.30 2
rs4309483 0.925 0.120 18 58418685 downstream gene variant A/C snv 0.70 2
rs4985790 0.925 0.120 17 21420842 downstream gene variant G/A snv 2
rs7000921 0.925 0.080 8 20535695 intergenic variant T/C snv 0.30 2
rs7755597 0.925 0.200 6 32738703 upstream gene variant C/T snv 0.80 2
rs7773068 0.925 0.200 6 32738457 upstream gene variant G/A;T snv 2
rs9268606 0.925 0.200 6 32432293 TF binding site variant G/A;T snv 2
rs9268607 0.925 0.200 6 32432761 regulatory region variant A/G snv 0.38 2
rs9276279 0.925 0.200 6 32734721 upstream gene variant C/T snv 0.80 2
rs9276298 0.925 0.200 6 32735244 upstream gene variant G/A snv 0.80 2