Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62557312 0.925 0.080 9 6047765 intron variant C/T snv 0.15 2
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs2544026
HDAC7
0.925 0.080 12 47792780 non coding transcript exon variant T/A snv 0.19 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs1117490
TRIM26
0.925 0.080 6 30202733 intron variant T/C snv 0.24 2
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs7183955
RORA
0.925 0.080 15 60757370 intron variant A/C snv 0.24 2
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 2
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs705699
SUOX ; RAB5B
0.882 0.160 12 55991020 non coding transcript exon variant G/A snv 0.40 5