Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs2890565
UTS2
0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13