Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61211515 1.000 0.120 6 30133199 upstream gene variant TT/-;T;TTT;TTTT delins 0.14 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs7775397
TSBP1-AS1 ; TSBP1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7
rs3136534 0.807 0.240 4 122448621 downstream gene variant T/G snv 0.29 6
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 5
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 4
rs10484566
PSMB9
0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs11014284
CACNB2
0.925 0.240 10 18451155 intron variant T/G snv 0.20 2
rs11568563
SLCO1A2
0.925 0.240 12 21304500 missense variant T/G snv 4.5E-02 4.4E-02 2
rs1223438908
CBLB
1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs3130817 0.925 0.160 6 29211460 upstream gene variant T/G snv 0.22 2
rs3132453
PRRC2A
0.925 0.200 6 31636267 missense variant T/G snv 0.96 0.95 2
rs752455542
CBLB
1.000 0.120 3 105681740 missense variant T/G snv 4.0E-06 2
rs1012411 1.000 0.120 6 30364778 upstream gene variant T/G snv 0.32 1
rs11052552
LINC02390
1.000 0.120 12 9703362 upstream gene variant T/G snv 0.42 1
rs1217419
AP4B1-AS1 ; PTPN22
1.000 0.120 1 113859282 intron variant T/G snv 0.56 1
rs13415583
AFF3
1.000 0.120 2 100147625 intron variant T/G snv 0.37 1