Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 6 | ||||
rs11021221 | 11 | 95575690 | intron variant | T/A;G | snv | 4 | |||||
rs113635136 | 3 | 196075973 | intron variant | AA/-;A;AAA;AAAA | delins | 3 | |||||
rs11672387 | 19 | 12870439 | intron variant | C/G | snv | 0.24 | 3 | ||||
rs1175550 | 1 | 3774964 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs12050884 | 15 | 40014133 | intron variant | C/A | snv | 0.25 | 4 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs131656 | 22 | 21563161 | intron variant | G/A | snv | 0.20 | 3 | ||||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 10 | |||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 6 | ||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 6 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 11 | |||||
rs2022003 | 1 | 158617176 | intron variant | A/T | snv | 0.28 | 5 | ||||
rs225245 | 17 | 35619088 | intron variant | A/G | snv | 0.39 | 3 | ||||
rs2748425 | 17 | 78128765 | 5 prime UTR variant | G/C | snv | 0.26 | 3 | ||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 4 | ||||
rs3169166 | 15 | 78270761 | intron variant | A/C | snv | 0.42 | 3 | ||||
rs3785309 | 16 | 162650 | intron variant | C/T | snv | 0.10 | 3 | ||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs415895 | 11 | 9748015 | missense variant | C/G | snv | 0.62 | 0.61 | 6 | |||
rs4737010 | 8 | 41772929 | intron variant | G/A | snv | 0.32 | 6 | ||||
rs57467915 | 2 | 219216694 | missense variant | G/A | snv | 8.8E-03 | 9.6E-03 | 3 | |||
rs59616136 | 19 | 17141231 | intron variant | G/A | snv | 8.1E-02 | 4 |