Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10067881 5 95826771 upstream gene variant G/A snv 9.4E-02 1
rs10449752 1 56152275 intron variant T/A;G snv 1
rs10710459 1 56467292 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA;AAAAAAAA delins 0.87 1
rs10954464 7 134700205 intergenic variant T/A snv 0.34 1
rs111373852 6 6679939 downstream gene variant -/TTAG delins 0.54 1
rs112062732 6 32486159 intergenic variant T/C;G snv 1
rs11438927 12 120746070 intron variant -/C ins 0.42 1
rs11678584 2 32338357 intergenic variant A/T snv 0.12 1
rs11686934 2 69944984 downstream gene variant A/G snv 0.43 1
rs11687659 2 190876471 upstream gene variant C/A snv 0.46 1
rs116896792 12 122464360 TF binding site variant T/C snv 5.9E-02 1
rs11961980 6 30794357 downstream gene variant C/T snv 2.7E-02 1
rs11967684 6 31231989 intergenic variant G/A snv 0.43 1
rs12140703 1 205213737 upstream gene variant G/C snv 0.27 1
rs12547135 8 71601857 intergenic variant T/C snv 0.39 1
rs12893668 14 103551456 upstream gene variant G/A snv 0.28 1
rs13101482 4 143989463 intron variant G/A snv 0.69 1
rs13300853 9 16901230 intergenic variant C/T snv 0.40 1
rs144215134 5 76773183 regulatory region variant A/C snv 2.6E-02 1
rs146563863 17 19994250 intergenic variant TTTTTTTT/-;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTTTTTT delins 0.21 1
rs1650507 5 158603805 intergenic variant G/A snv 0.23 1
rs17187854 6 30097766 intergenic variant A/T snv 4.5E-03 1
rs17462893 5 95827733 downstream gene variant A/G snv 0.13 1
rs1797885 3 12475604 intergenic variant G/A snv 0.66 1
rs1936799 6 127112993 intron variant C/T snv 0.33 1