Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 10
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 8
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 8
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs937475913
PRKDC
0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 6
rs1064794272
VHL
0.807 0.240 3 10146566 missense variant C/A snv 6
rs1131691061
SDHB
0.827 0.280 1 17054017 start lost C/T snv 6
rs137853236
HNF1A
0.807 0.280 12 120997504 missense variant C/T snv 1.2E-05 6
rs1555212014
HNF1A
0.807 0.280 12 120994264 missense variant C/T snv 6
rs17037102
DKK2
0.807 0.240 4 106924637 missense variant C/A;T snv 0.15 6
rs5030820
VHL
0.827 0.280 3 10149822 missense variant C/G;T snv 8.0E-06 6