Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3829251 0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs222020
GC
0.851 0.320 4 71770555 intron variant C/T snv 0.72 5
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs2118610 1.000 0.080 15 67135996 intron variant T/C snv 0.59 2
rs4945008 1.000 0.080 11 71510202 intron variant A/G;T snv 2
rs7116978 1.000 0.080 11 14860225 intron variant T/C snv 0.65 2
rs587777606 0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs756632799 0.882 0.080 20 45416579 stop gained G/T snv 1.6E-05 7.0E-06 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1064797245 0.776 0.280 19 41970540 missense variant G/A snv 12
rs143319805 0.807 0.320 3 193643378 missense variant A/G snv 6.2E-04 5.7E-04 12
rs74315403 0.790 0.200 20 4699752 missense variant G/A snv 10
rs796052676 0.807 0.200 8 132180246 missense variant G/A snv 10
rs118192211 0.790 0.080 20 63439644 missense variant G/A;C snv 9
rs587776983 0.807 0.240 19 6502209 missense variant G/A;C;T snv 9
rs1057516085 0.827 0.080 20 63444747 missense variant C/T snv 8
rs1799821 0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs2229291 0.827 0.200 1 53210729 missense variant T/G snv 2.3E-02 1.5E-02 8