Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893626
CXCR4 ; LOC112268426
0.827 0.280 2 136114915 stop gained G/C snv 11
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 4
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs12144309
RSBN1
1 113772871 intron variant C/T snv 0.19 1
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs141185042
DNM1L
12 32707409 missense variant A/T snv 4.1E-06 7.0E-06 1
rs1472503583
PWWP3A
0.925 0.160 19 1360712 missense variant C/T snv 4.0E-06 4
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs149627368
REL
2 60922344 missense variant T/C snv 1.5E-04 1.0E-04 1
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs1799725
SOD2
6 159692840 missense variant A/G snv 1
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs2227945
BRCA1
1.000 0.080 17 43092113 missense variant T/C;G snv 2.5E-03 1.0E-02 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6