Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10243492 1.000 0.080 7 32780825 intergenic variant A/G snv 0.48 1
rs10484569 1.000 0.080 6 33091175 downstream gene variant G/A snv 5.9E-02 1
rs11638027 1.000 0.080 15 90302268 intron variant G/T snv 9.9E-02 1
rs12649554 1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65 1
rs12979680 1.000 0.080 19 21691444 intergenic variant C/A;T snv 1
rs154977 1.000 0.080 6 32932241 downstream gene variant C/G;T snv 1
rs17056316 1.000 0.080 4 170892334 downstream gene variant A/G snv 2.6E-03 1
rs2395223 1.000 0.080 6 32614001 intergenic variant C/T snv 0.44 1
rs2395535 1.000 0.080 6 32689574 TF binding site variant A/C;G snv 1
rs2646996 1.000 0.080 6 32697964 intergenic variant A/G snv 0.34 1
rs2647047 1.000 0.080 6 32700927 regulatory region variant C/G snv 0.34 1
rs2708973 1.000 0.080 2 112906296 intergenic variant A/G snv 0.96 1
rs2856664 1.000 0.080 6 32697839 intergenic variant G/T snv 0.34 1
rs2856704 1.000 0.080 6 32703237 downstream gene variant C/A snv 0.34 1
rs2856720 1.000 0.080 6 32700880 regulatory region variant C/T snv 0.34 1
rs2858859 1.000 0.080 6 32614498 intergenic variant G/A snv 0.43 1
rs2894316 1.000 0.080 6 33098817 upstream gene variant A/G snv 0.57 1
rs3129987 1.000 0.080 6 30798427 downstream gene variant T/A;C snv 1
rs3134996 1.000 0.080 6 32669089 upstream gene variant A/T snv 0.62 1
rs3135402 1.000 0.080 6 33056877 regulatory region variant A/C snv 0.35 1
rs34937821 1.000 0.080 6 33058776 regulatory region variant G/A snv 0.28 1
rs4365966 1.000 0.080 6 31263941 downstream gene variant C/A;G snv 1
rs4538748 1.000 0.080 6 32689728 TF binding site variant T/C snv 0.41 1
rs5004276 1.000 0.080 6 32614555 intergenic variant G/A snv 0.43 1
rs555627 1.000 0.080 6 159538641 intron variant G/A snv 7.6E-02 1