Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs975730 8 128303768 intergenic variant G/A snv 0.45 2
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs9507287
SPATA13
0.851 0.040 13 24212439 intron variant T/C snv 0.24 5
rs945635
FCRL3
0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs9356551 0.882 6 166986857 intron variant T/C snv 0.42 4
rs934734
SPRED2
0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 4
rs9295089
LOC105378083 ; TAGAP
6 159042932 non coding transcript exon variant T/C snv 0.20 2
rs926657
TAGAP ; LOC105378083
6 159042420 non coding transcript exon variant C/G;T snv 3
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs8734
TTTY14
Y 18992540 non coding transcript exon variant G/A snv 1
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs8176928
TRAP1 ; DNASE1
16 3656184 missense variant A/G snv 1.0E-03 4.0E-03 1