Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs730882018
TP53
0.851 0.320 17 7676153 frameshift variant G/-;GG delins 5
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 4
rs34562254
TNFRSF13B
1.000 0.160 17 16939677 missense variant G/A snv 0.14 0.12 3
rs57968458 0.882 0.160 17 16916785 intergenic variant G/A snv 0.15 3
rs2302777
MED24
0.925 0.200 17 40023239 synonymous variant A/G snv 0.39 0.30 2
rs8070529
CACNG4
0.925 0.200 17 66986976 intron variant C/A;T snv 4.2E-02 2
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs2107356
IL4R
0.851 0.240 16 27312083 upstream gene variant C/T snv 0.35 4
rs4240803
SLC7A5 ; LOC107987237
0.851 0.240 16 87855597 intron variant G/A;C;T snv 4
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs7193541
RFWD3
1.000 0.160 16 74630845 missense variant T/C snv 0.37 0.43 2
rs13338946 1.000 0.160 16 30689537 intergenic variant T/C;G snv 1
rs72773978
FOPNL
1.000 0.160 16 15880785 intron variant A/T snv 8.1E-02 1
rs8058578
SRCAP
1.000 0.160 16 30714927 intron variant C/T snv 0.32 1
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4