Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 5
rs13202464 0.925 0.040 6 31376806 upstream gene variant A/G snv 6.3E-02 5
rs4418214 0.925 0.040 6 31423624 intron variant T/C snv 7.7E-02 5
rs9265882
HLA-B
0.925 0.040 6 31345324 intron variant T/C snv 0.35 5
rs17524488
SPP1
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins 4
rs10045403
ERAP1
0.882 0.040 5 96812030 upstream gene variant A/G snv 0.23 3
rs715572
TIMP3 ; SYN3
0.925 0.040 22 32838944 intron variant G/A snv 0.18 3
rs8176786
NELL1
0.925 0.040 11 20937848 missense variant C/T snv 4.5E-02 3.7E-02 3
rs10440635 1.000 0.040 5 40490688 intron variant G/A snv 0.56 2
rs10489630
C1orf141 ; IL23R
0.925 0.040 1 67196939 intron variant A/C;T snv 2
rs1061680
LILRB1
1.000 0.040 19 54632001 missense variant C/T snv 2
rs11065898
SH2B3
1.000 0.040 12 111424771 intron variant C/T snv 0.21 2
rs12504282
ANTXR2
1.000 0.040 4 80005847 intron variant C/G;T snv 2
rs13210693
CCDC162P
1.000 0.040 6 109277761 intron variant G/A snv 0.61 2
rs14335
FCRL4
1.000 0.040 1 157575060 3 prime UTR variant C/T snv 0.32 2
rs17095830
ANO6
1.000 0.040 12 45381125 intron variant A/G snv 7.9E-02 2
rs1894399
IL1A
0.925 0.040 2 112782600 intron variant C/T snv 0.32 2
rs2621332
HLA-DOB
0.925 0.040 6 32812540 downstream gene variant G/A snv 0.67 2
rs35164067
CDC37
1.000 0.040 19 10414505 intron variant G/A snv 0.18 2
rs3750996
STIM1
1.000 0.040 11 4091970 3 prime UTR variant A/G snv 7.7E-03 2
rs3811058
IL1F10
0.925 0.040 2 113074368 missense variant T/A;C snv 4.0E-06; 0.13 2
rs4349859
MICA-AS1
0.925 0.040 6 31398010 upstream gene variant G/A snv 3.1E-02 2
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 2
rs4792909 1.000 0.040 17 43721456 upstream gene variant G/T snv 0.51 2
rs6556416 1.000 0.040 5 159391737 intron variant A/C;T snv 2