Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 7
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 5
rs582054
IL12A ; IL12A-AS1
0.882 0.160 3 159992214 intron variant A/C;T snv 5
rs1264457
HLA-E
0.851 0.160 6 30490287 missense variant G/A;T snv 0.54 4
rs12524487 0.925 0.160 6 31386461 upstream gene variant C/T snv 5.9E-02 3
rs8111
ATF6B ; TNXB
0.925 0.160 6 32115398 3 prime UTR variant C/T snv 0.26 3
rs665268
MLX
0.882 0.160 17 42570011 missense variant A/G snv 0.28 0.25 3
rs10919543 1.000 0.080 1 161538827 intron variant A/G snv 0.28 2
rs2099684 1.000 0.080 1 161530340 intron variant A/G snv 0.28 2
rs4817984 1.000 0.080 21 39093140 intergenic variant C/A;G snv 2
rs4921492 0.925 0.120 5 159405269 intron variant C/A;G snv 2
rs4921493 0.925 0.080 5 159409099 intron variant T/A;C snv 2
rs9366782 1.000 0.080 6 31360768 upstream gene variant A/T snv 9.4E-02 2
rs1383258
HLA-DOB
0.925 0.160 6 32815628 intron variant C/T snv 8.3E-02 2
rs3763288
MICA
0.925 0.160 6 31402590 non coding transcript exon variant G/A snv 5.3E-02 2
rs104895476
NOD2
0.925 0.160 16 50711057 missense variant C/G;T snv 4.8E-05 2