Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 3
rs2618479
BLK
0.925 0.280 8 11498312 intron variant A/G snv 0.84 2
rs10817595
AKNA
0.925 0.200 9 114361470 intron variant C/A;T snv 0.41 2
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
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
rs11575837
NCR3
1.000 0.200 6 31592893 5 prime UTR variant C/T snv 2.4E-02 2
rs2839698
MRPL23 ; MIR675 ; H19
0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs201802880
NCF1
0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs3135945
TREX1 ; ATRIP ; ATRIP-TREX1 ; SHISA5
1.000 0.200 3 48467567 synonymous variant G/A snv 9.4E-03 4.0E-02 2
rs1376314937
AKNA
1.000 0.200 9 114361709 missense variant G/A snv 4.0E-06 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11