Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14