Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 6
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 6
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 5
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 5
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 4
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 3
rs2040406
HLA-DQA1
0.882 0.240 6 32635230 intron variant A/G snv 0.23 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25 3
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 3
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 3
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 3
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 2
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 2
rs10272859
CDK14
0.925 0.120 7 90689160 intron variant G/C snv 0.39 2
rs10485505
ITCH
1.000 0.080 20 34437762 intron variant C/G;T snv 2
rs10931481
STAT4
0.827 0.240 2 191090126 intron variant G/A snv 0.66 2
rs11866328
GRIN2A
0.925 0.120 16 9768699 intron variant G/T snv 0.38 2
rs171915
LOC153910
1.000 0.080 6 142545708 intron variant G/A snv 0.22 2