Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs604714
DPAGT1
0.925 0.120 11 119099986 intron variant C/A snv 0.31 3
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs6857600
ABCG2
0.925 0.120 4 88144923 intron variant C/T snv 0.28 3
rs3789607
AP4B1-AS1 ; PTPN22
1 113823812 intron variant T/C snv 0.21 1
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs12144309
RSBN1
1 113772871 intron variant C/T snv 0.19 1
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs3811021
AP4B1-AS1 ; PTPN22 ; RSBN1
1.000 0.080 1 113814041 3 prime UTR variant A/G snv 0.15 2
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
rs3218674
ATM
1.000 0.120 11 108244860 synonymous variant C/G;T snv 1.1E-02 1.1E-02 2
rs2227945
BRCA1
1.000 0.080 17 43092113 missense variant T/C;G snv 2.5E-03 1.0E-02 2
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs149627368
REL
2 60922344 missense variant T/C snv 1.5E-04 1.0E-04 1
rs141185042
DNM1L
12 32707409 missense variant A/T snv 4.1E-06 7.0E-06 1
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490