Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11038689
CRY2
0.882 0.160 11 45852713 intron variant A/G snv 0.19 3
rs1401417
CRY2
0.882 0.160 11 45858559 intron variant C/G snv 0.19 3
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs7123390
CRY2
0.882 0.160 11 45869867 intron variant G/A snv 0.22 0.22 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs207186 0.925 0.120 1 55359252 intron variant C/T snv 7.7E-03 2
rs2855429
COL11A2
0.925 0.120 6 33190412 intron variant A/C snv 0.78 2
rs3789068
MIR4435-2HG ; BCL2L11
0.925 0.120 2 111151670 intron variant A/G snv 0.41 2
rs4661636
CASP9
0.925 0.160 1 15496566 intron variant C/T snv 0.24 2
rs13178127
XRCC4
1.000 0.120 5 83293613 intron variant A/G snv 3.3E-02 1
rs16994592
CD70
1.000 0.120 19 6586487 intron variant T/C snv 9.4E-02 1
rs1785882
CARD16 ; LOC107984381
1.000 0.120 11 105052348 intron variant A/T snv 0.45 1
rs1800893
IL19 ; IL10
1.000 0.120 1 206773822 intron variant C/T snv 0.41 1
rs1921310
TANK
1.000 0.120 2 161192690 intron variant A/G snv 0.15 1
rs2237060
RAD50 ; TH2LCRR
1.000 0.120 5 132635193 intron variant T/G snv 0.29 1
rs2582869
TNFSF13B
1.000 0.120 13 108259797 intron variant A/G;T snv 1
rs2637988
IL1RN
1.000 0.120 2 113119202 intron variant G/A snv 0.53 1
rs2991216
SYK
1.000 0.120 9 90865745 intron variant A/G snv 0.21 1
rs4648022
NFKB1
1.000 0.120 4 102575280 intron variant C/A;T snv 1
rs6002551
CENPM
1.000 0.120 22 41942148 intron variant G/A snv 0.20 1
rs6736233
CASP8
1.000 0.120 2 201254251 intron variant G/C snv 0.16 1
rs78440425
CXCR5
1.000 0.120 11 118888302 intron variant G/A snv 1.1E-02 1
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6