Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 1
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs9501626 0.925 0.200 6 32432567 regulatory region variant C/A snv 0.18 2
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs9469583
IP6K3
1.000 0.120 6 33749993 upstream gene variant T/C snv 0.52 1
rs9469566
UQCC2
1.000 0.120 6 33699828 intron variant C/A snv 0.41 1
rs9469084
TNXB
1.000 0.120 6 32112606 non coding transcript exon variant C/T snv 0.12 1
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 4
rs942643
UQCC2
1.000 0.120 6 33700593 intron variant A/G snv 0.41 1
rs942152
RAB14
1.000 0.120 9 121189407 intron variant C/A;T snv 1
rs9405112 1.000 0.120 6 32477823 upstream gene variant G/A;T snv 2
rs9405090
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32330595 missense variant A/G snv 0.42 0.33 2
rs9405040
HLA-DRB9
1.000 0.120 6 32471616 intron variant A/C;T snv 2
rs9394169 1.000 0.120 6 33811187 regulatory region variant A/G snv 0.52 1
rs9391786 1.000 0.120 6 32480784 intergenic variant A/G snv 1
rs9380254
MICA
1.000 0.120 6 31410558 missense variant G/A;C snv 5.7E-05; 7.8E-02 1
rs9380167
HCG17 ; HCG18
1.000 0.120 6 30306684 non coding transcript exon variant A/G snv 0.32 1
rs9378815 1.000 0.120 6 426155 intergenic variant G/A;C;T snv 1
rs9378266 1.000 0.120 6 32480412 intergenic variant G/C;T snv 1
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 2
rs9378213 0.925 0.160 6 32480621 intergenic variant T/A;G snv 2
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 2
rs9378109
LINC00243
0.925 0.120 6 30806697 intron variant C/A snv 0.16 5
rs9373594
PPIL4
1.000 0.120 6 149513438 intron variant T/A;C snv 1
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 1