Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1376314937
AKNA
1.000 0.200 9 114361709 missense variant G/A snv 4.0E-06 1
rs10817595
AKNA
0.925 0.200 9 114361470 intron variant C/A;T snv 0.41 2
rs2618479
BLK
0.925 0.280 8 11498312 intron variant A/G snv 0.84 2
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs11575837
NCR3
1.000 0.200 6 31592893 5 prime UTR variant C/T snv 2.4E-02 2
rs3135945
TREX1 ; ATRIP ; ATRIP-TREX1 ; SHISA5
1.000 0.200 3 48467567 synonymous variant G/A snv 9.4E-03 4.0E-02 2
rs10840759
CLEC4A
0.882 0.200 12 8138610 intron variant C/T snv 0.28 3
rs2377422
CLEC4A
0.882 0.200 12 8128312 intron variant C/T snv 0.60 3
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 3
rs4522865
BANK1
0.882 0.240 4 101794731 intron variant G/A;T snv 4
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 4
rs201802880
NCF1
0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs13447
NCF1C
0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs2070197
IRF5
0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10