Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs773862672
MTOR
0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs3811021
AP4B1-AS1 ; PTPN22 ; RSBN1
1.000 0.080 1 113814041 3 prime UTR variant A/G snv 0.15 2
rs12144309
RSBN1
1 113772871 intron variant C/T snv 0.19 1
rs3789607
AP4B1-AS1 ; PTPN22
1 113823812 intron variant T/C snv 0.21 1
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
rs104893626
CXCR4 ; LOC112268426
0.827 0.280 2 136114915 stop gained G/C snv 11
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs149627368
REL
2 60922344 missense variant T/C snv 1.5E-04 1.0E-04 1
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs764643047
OGG1
0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 5
rs6857600
ABCG2
0.925 0.120 4 88144923 intron variant C/T snv 0.28 3
rs355689
LOC105377296 ; CXCL13
1.000 0.040 4 77586643 intron variant T/A;C snv 2
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs1799725
SOD2
6 159692840 missense variant A/G snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157