Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 4
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 3
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs17876205 7 95403792 downstream gene variant C/G snv 1.4E-02 1
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs926657
TAGAP ; LOC105378083
6 159042420 non coding transcript exon variant C/G;T snv 3
rs756207760
CXCR4
2 136115275 missense variant C/G;T snv 4.0E-06; 4.0E-06 2
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 10
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 9
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5