Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs10994982 0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs121909646 0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs17213693 0.925 0.120 6 32813344 intron variant G/C snv 9.8E-02 2
rs9479
PML
0.851 0.120 15 74036235 3 prime UTR variant A/G snv 0.50 6
rs762613037 0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs11545078
GGH
0.807 0.200 8 63026205 missense variant G/A snv 8.8E-02 7.8E-02 6
rs7089424 0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs1470755915 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs2239633 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs797045145 0.807 0.240 6 26091479 stop gained G/A snv 6
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs2735383 0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs780246573 0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs80338880 0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12