Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs2070197
IRF5
0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
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
rs2839698
MRPL23 ; MIR675 ; H19
0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs13447
NCF1C
0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs201802880
NCF1
0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs1376314937
AKNA
1.000 0.200 9 114361709 missense variant G/A snv 4.0E-06 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6