Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799821 0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs1255283120 0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs12090554 0.925 0.080 1 185583216 intron variant G/A snv 0.15 2
rs12095080 1.000 0.080 1 53911057 3 prime UTR variant A/G snv 0.12 2
rs6125 0.925 0.080 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 2
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs199473244 0.851 0.120 3 38557251 missense variant C/A snv 4
rs200034939 0.882 0.080 3 38557248 missense variant C/A snv 3.2E-05 3
rs1049194905 0.925 0.080 3 38604063 synonymous variant A/G snv 2
rs1237080661 0.925 0.080 3 38604780 stop gained A/G;T snv 2.8E-05 2
rs184934308 0.925 0.080 3 38575342 synonymous variant G/A snv 4.1E-04 9.1E-05 2
rs750678689 0.925 0.080 3 38566466 synonymous variant G/A snv 8.0E-06 2.1E-05 2
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs4220
FGB
0.925 0.080 4 154570607 missense variant G/A snv 0.17 0.15 6