Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
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
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 4
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs604714
DPAGT1
0.925 0.120 11 119099986 intron variant C/A snv 0.31 3
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
rs3811021
AP4B1-AS1 ; PTPN22 ; RSBN1
1.000 0.080 1 113814041 3 prime UTR variant A/G snv 0.15 2
rs539846
BMF
1.000 0.120 15 40105735 intron variant G/C;T snv 2
rs12144309
RSBN1
1 113772871 intron variant C/T snv 0.19 1
rs1799725
SOD2
6 159692840 missense variant A/G snv 1
rs3789607
AP4B1-AS1 ; PTPN22
1 113823812 intron variant T/C snv 0.21 1