Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs10840759
CLEC4A
0.882 0.200 12 8138610 intron variant C/T snv 0.28 3
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 4
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs10817595
AKNA
0.925 0.200 9 114361470 intron variant C/A;T snv 0.41 2
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2377422
CLEC4A
0.882 0.200 12 8128312 intron variant C/T snv 0.60 3
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs2618479
BLK
0.925 0.280 8 11498312 intron variant A/G snv 0.84 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121