Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs260020
ZNF831
1.000 0.040 20 59138970 intron variant C/T snv 0.20 1
rs35879803
ZNF827
1.000 0.040 4 145861685 non coding transcript exon variant C/A;T snv 1
rs4345206
ZNF827
1.000 0.040 4 145845384 intron variant T/C snv 0.59 1
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs62076439
ZNF652
1.000 0.040 17 49327266 intron variant G/A;T snv 1
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs16998248
ZNF217
0.882 0.040 20 53581801 synonymous variant T/A snv 0.11 8.8E-02 3
rs35720349
ZNF217
0.882 0.040 20 53577121 missense variant G/A snv 3.4E-02 1.6E-02 3
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs8103163
ZNF208
0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs2188971
ZNF208
0.925 0.080 19 21969380 3 prime UTR variant T/A;C snv 2
rs6102343
ZHX3
1.000 0.040 20 41295639 intron variant G/A snv 0.29 1
rs2342781
ZFPM2
1.000 0.040 8 105253492 intron variant C/G;T snv 1
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02 4
rs6740731
ZEB2
1.000 0.040 2 144513025 3 prime UTR variant G/A;C;T snv 0.25 1
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs4739066
YTHDF3
0.925 0.080 8 63191534 intron variant A/G snv 0.12 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs498186
WTAPP1 ; MMP1
0.925 0.080 11 102798914 intron variant A/C snv 0.40 2