Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs4522865
BANK1
0.882 0.240 4 101794731 intron variant G/A;T snv 4
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs13447
NCF1C
0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs2070197
IRF5
0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 4