Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3135945
TREX1 ; ATRIP ; ATRIP-TREX1 ; SHISA5
1.000 0.200 3 48467567 synonymous variant G/A snv 9.4E-03 4.0E-02 2
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 3
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4522865
BANK1
0.882 0.240 4 101794731 intron variant G/A;T snv 4
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 4
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12