Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13116227 1.000 0.080 4 8556539 upstream gene variant C/G;T snv 1
rs13332649 1.000 0.080 16 85933077 intron variant A/G snv 0.18 1
rs13344313 1.000 0.080 19 18406957 regulatory region variant G/A snv 0.31 1
rs137956 1.000 0.080 22 39897459 upstream gene variant C/A;T snv 1
rs150518861 1.000 0.080 7 74152347 intergenic variant G/A snv 1.0E-02 1
rs1634318 1.000 0.080 X 12891359 downstream gene variant A/G snv 0.24 1
rs16895070 1.000 0.080 6 29553780 missense variant T/C snv 0.16 1
rs17184255 1.000 0.080 6 29553512 synonymous variant C/G snv 0.16 1
rs17552904 1.000 0.080 7 50278712 upstream gene variant G/T snv 0.22 1
rs205284 1.000 0.080 6 34584135 downstream gene variant C/G;T snv 1
rs2084654 1.000 0.080 7 129089074 intergenic variant A/G snv 0.39 1
rs223883 1.000 0.080 16 57354818 upstream gene variant G/A snv 0.65 1
rs2341697 1.000 0.080 2 238212011 intergenic variant T/C snv 0.40 1
rs2532871 1.000 0.080 X 30555616 downstream gene variant G/C snv 1
rs2844580 1.000 0.080 6 31365526 upstream gene variant T/C snv 0.32 1
rs2934498 1.000 0.080 16 85934676 intron variant A/G snv 0.35 1
rs2980512 1.000 0.080 8 8283379 intergenic variant T/C snv 0.40 1
rs3129716 1.000 0.080 6 32689659 TF binding site variant T/C snv 9.8E-02 1
rs3129975 1.000 0.080 6 30764277 intron variant T/C;G snv 1
rs332398 1.000 0.080 1 161566341 intron variant C/T snv 0.44 1
rs34889541 1.000 0.080 1 198625639 intergenic variant G/A snv 6.3E-02 1
rs36014129 1.000 0.080 6 25884291 upstream gene variant G/A snv 4.6E-02 1
rs387619 1.000 0.080 11 35076646 intergenic variant T/A;C snv 1
rs4382707 1.000 0.080 1 242802070 intergenic variant G/A snv 0.27 1
rs4684256 1.000 0.080 3 1590669 intergenic variant C/A;G;T snv 1