Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7178239 1.000 0.040 15 101267907 downstream gene variant C/G snv 0.37 2
rs2009895
SELENOS
1.000 0.040 15 101276024 intron variant C/A;T snv 3.0E-02 1
rs28665122
SELENOS
0.807 0.240 15 101277522 upstream gene variant C/T snv 0.24 7
rs165501
IRAK2
1.000 0.040 3 10167559 intron variant T/A;C snv 1
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs6543116
IL1RL1
0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76 3
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs111033243
SLC26A4
0.827 0.400 7 107689112 missense variant T/C snv 6.1E-04 8.1E-04 5
rs7537605
VAV3
0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs12730735
AP4B1-AS1 ; PTPN22
1.000 0.040 1 113838835 intron variant T/C snv 0.21 1
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs6972286 1.000 0.040 7 118685680 intergenic variant A/T snv 0.43 2
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3