Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs907715 0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs2516509 0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3129871 0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs479536 0.882 0.200 6 32225901 upstream gene variant G/A snv 5.0E-02 3
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6