Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs17339836
TNPO3
1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 1
rs6579837
TNIP1
1.000 0.200 5 151055333 intron variant G/T snv 0.11 1
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 1
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs17074492
LOC105370283
1.000 0.200 13 81587764 intergenic variant C/A;T snv 1
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs11048434
KLRG1
1.000 0.200 12 9001336 intron variant G/A snv 0.28 1
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6
rs3823536
IRF5
0.925 0.280 7 128939612 intron variant G/A snv 0.40 2
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5