Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs3811021
AP4B1-AS1 ; PTPN22 ; RSBN1
1.000 0.080 1 113814041 3 prime UTR variant A/G snv 0.15 2
rs1799725
SOD2
6 159692840 missense variant A/G snv 1
rs141185042
DNM1L
12 32707409 missense variant A/T snv 4.1E-06 7.0E-06 1
rs604714
DPAGT1
0.925 0.120 11 119099986 intron variant C/A snv 0.31 3
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs3218674
ATM
1.000 0.120 11 108244860 synonymous variant C/G;T snv 1.1E-02 1.1E-02 2
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs764643047
OGG1
0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 5
rs1472503583
PWWP3A
0.925 0.160 19 1360712 missense variant C/T snv 4.0E-06 4
rs6857600
ABCG2
0.925 0.120 4 88144923 intron variant C/T snv 0.28 3
rs12144309
RSBN1
1 113772871 intron variant C/T snv 0.19 1
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151