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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 8
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs6672420
LOC105376878 ; RUNX3
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50 6
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs2208568
LOC105373215 ; LINC02768
1 235926855 intergenic variant T/A;C;G snv 5
rs3917914
CSF3R
1 36482287 intron variant G/A;T snv 5
rs3917932
CSF3R
1 36478315 intron variant C/G snv 0.59 5
rs663045
SLC25A24
1 108200437 5 prime UTR variant G/C snv 0.55 5
rs7550207
CADM3-AS1 ; ACKR1
1 159205095 intron variant T/C snv 0.19 5
rs9436747
LEPR
1 65445924 intron variant T/C snv 0.56 5
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs11211480
TAL1
1 47227548 non coding transcript exon variant A/G snv 0.42 4
rs34293785 1 65671509 intergenic variant T/C snv 4
rs41313381
ADGRL4
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05 4
rs4844622
MIR29B2CHG
1 207860984 intron variant C/T snv 0.19 4
rs4951378
ATP2B4
1 203689654 intron variant A/G snv 0.83 4