Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3824662 0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs3792192 0.925 0.160 2 160030364 intron variant G/A snv 0.35 2
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs329498 0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs292001 0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs28940579 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs274068 0.925 0.160 16 24887651 intron variant C/A snv 0.74 2
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs2298804 0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs2295415 0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1
rs2246614 0.882 0.160 11 619789 missense variant T/G snv 0.63 0.59 3
rs2157257 1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs17008504 1.000 0.160 4 124718662 intergenic variant T/A snv 4.3E-02 1
rs1635564 0.925 0.160 1 17357031 intron variant T/A;G snv 2
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5