Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs16999593
DNMT1
0.742 0.240 19 10180505 missense variant T/C snv 2.4E-02 9.6E-03 14
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 10
rs3138053
NFKBIA
0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 10
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs780634396
BCL2
0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs781490101
TP53
0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs11651270
NLRP1
0.882 0.240 17 5521757 missense variant T/C snv 0.45 0.47 4
rs1452231640
POLB
1.000 0.080 8 42339015 missense variant T/C snv 4.0E-06 4
rs7214723
CAMKK1
0.882 0.080 17 3872554 missense variant T/C snv 0.45 0.36 4
rs765189442
ABCB11
0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06 4
rs1259653415
TFRC
1.000 0.080 3 196071416 missense variant T/C snv 7.0E-06 3
rs74751600
CHEK2
22 28695852 missense variant T/C snv 3
rs1374712964
MUTYH
1.000 0.080 1 45332028 missense variant T/C snv 2
rs1390902532
CDKN2A
1.000 0.040 9 21968766 missense variant T/C snv 7.4E-06 7.0E-06 2
rs373646414
DICER1
1.000 0.080 14 95132574 missense variant T/C snv 1.6E-05 5.6E-05 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs267601394
EZH2
0.807 0.200 7 148811635 missense variant T/A;G snv 8
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88