Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 8
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 8
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 7
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 7
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 7
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7