Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs1534430
MIR3681HG
0.851 0.040 2 12504610 intron variant C/T snv 0.35 5
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 4
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs6914622
SASH1
0.851 0.040 6 148193165 regulatory region variant G/T snv 0.33 5
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs1549922 0.882 5 159304540 intergenic variant G/A snv 0.56 4