Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35300242
ATG16L1
0.827 0.120 2 233260144 intron variant G/A;C snv 5
rs4456788
GATD3A
0.827 0.120 21 44196441 intron variant G/A snv 5
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5
rs4812833
LINC01620
0.827 0.120 20 44440356 intron variant G/A;C snv 5
rs4971079 0.827 0.120 1 155157915 intergenic variant G/A;C snv 5
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 5
rs5757584 0.827 0.120 22 39266545 intron variant C/G;T snv 5
rs59867199 0.827 0.120 4 122531076 intergenic variant C/G;T snv 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs6561151
NRAD1 ; LOC107984576
0.827 0.120 13 43910570 intron variant G/A;T snv 5
rs661054
NXPE1 ; NXPE2
0.827 0.120 11 114559688 intron variant A/G;T snv 5
rs702872
LINC01185
0.827 0.120 2 60854175 intron variant C/G;T snv 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs73178598
LOC105376976
0.827 0.120 3 18763719 intron variant T/C;G snv 5
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 5
rs76913543 0.827 0.120 10 6000052 intergenic variant G/A;C snv 5
rs7805114 0.827 0.120 7 107809588 downstream gene variant T/A;G snv 5
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 3
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 2
rs12602912
BPTF
1.000 0.040 17 67873957 intron variant C/G;T snv 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 2