Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs2457837
FRMD4A
1.000 0.080 10 14009457 intron variant C/T snv 0.38 1
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 5
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs4921492 0.925 0.120 5 159405269 intron variant C/A;G snv 2
rs60689680 1.000 0.080 5 159407359 intron variant G/T snv 0.31 1
rs4921493 0.925 0.080 5 159409099 intron variant T/A;C snv 2
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs582054
IL12A ; IL12A-AS1
0.882 0.160 3 159992214 intron variant A/C;T snv 5
rs2099684 1.000 0.080 1 161530340 intron variant A/G snv 0.28 2
rs10919543 1.000 0.080 1 161538827 intron variant A/G snv 0.28 2
rs12047961
LOC105371497
1.000 0.080 1 162479619 intergenic variant G/A snv 1.3E-02 1
rs10921544 1.000 0.080 1 194360431 intergenic variant C/G;T snv 1
rs1713450
KLHL33
1.000 0.080 14 20428086 3 prime UTR variant T/C snv 0.44 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs12608210 1.000 0.080 18 24913920 intron variant G/A snv 0.31 1
rs17133698 1.000 0.080 6 255562 regulatory region variant C/T snv 6.5E-02 1
rs2322599
PTK2B
1.000 0.080 8 27354393 intron variant G/A snv 0.38 1
rs4463283 1.000 0.080 6 29097215 upstream gene variant C/A;T snv 8.1E-02 1
rs9380141 1.000 0.080 6 29809899 downstream gene variant T/C snv 0.25 1
rs4713281
ZNRD1ASP
1.000 0.080 6 30010575 intron variant G/A snv 0.23 1
rs1264457
HLA-E
0.851 0.160 6 30490287 missense variant G/A;T snv 0.54 4
rs7743661
DDR1 ; MIR4640
1.000 0.080 6 30890477 non coding transcript exon variant T/C snv 0.25 1