Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8101626
DNMT1
1.000 0.120 19 10135353 intron variant G/A snv 0.64 1
rs779805
VHL
0.851 0.120 3 10141653 5 prime UTR variant G/A;C snv 4
rs776399733
VHL
0.882 0.120 3 10141965 missense variant C/A;T snv 6.5E-06 3
rs869025621
VHL
0.882 0.240 3 10142079 missense variant A/C;G;T snv 4
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04 4
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 10
rs397516440
VHL
0.851 0.280 3 10142166 missense variant C/G;T snv 4.5E-06 4
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 8
rs1064794272
VHL
0.807 0.240 3 10146566 missense variant C/A snv 6
rs1642743
VHL
1.000 0.120 3 10148783 intron variant C/G;T snv 1
rs28940297
VHL
0.882 0.240 3 10149811 missense variant T/C;G snv 4
rs5030820
VHL
0.827 0.280 3 10149822 missense variant C/G;T snv 8.0E-06 6
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 8
rs869025668
VHL
0.882 0.240 3 10149964 stop lost G/T snv 3
rs1642742
VHL
1.000 0.120 3 10150259 3 prime UTR variant G/A snv 0.57 1
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs5742714
IGF1 ; HELLPAR ; LINC02456
0.882 0.160 12 102396074 3 prime UTR variant C/G snv 8.9E-02 3
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 2
rs2297235
GSTO2
0.752 0.320 10 104274733 5 prime UTR variant A/G snv 0.22 11
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs6466135 0.925 0.120 7 106861053 upstream gene variant A/G snv 0.71 2
rs17037102
DKK2
0.807 0.240 4 106924637 missense variant C/A;T snv 0.15 6