Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs1108131
CAMK1D
0.925 0.160 10 12455748 intron variant T/C snv 0.28 2
rs1364989 0.925 0.160 4 54145602 intron variant T/C snv 0.73 2
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2246614
CDHR5
0.882 0.160 11 619789 missense variant T/G snv 0.63 0.59 3
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2