Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs66803065 | 11 | 10004305 | intron variant | C/A;T | snv | 0.19 | 2 | ||||
rs7158754 | 14 | 100117012 | intron variant | A/G | snv | 0.81 | 1 | ||||
rs67885470 | 11 | 100127699 | intron variant | C/T | snv | 0.18 | 1 | ||||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs1535464 | 14 | 100327094 | intron variant | G/A | snv | 0.18 | 2 | ||||
rs26030 | 5 | 100542328 | intron variant | T/C | snv | 0.61 | 1 | ||||
rs35571646 | 11 | 100662632 | upstream gene variant | -/CTAT | ins | 0.34 | 1 | ||||
rs1693567 | 8 | 100665158 | upstream gene variant | T/C | snv | 0.61 | 1 | ||||
rs670401 | 11 | 100701679 | intron variant | A/G | snv | 0.76 | 3 | ||||
rs6590811 | 11 | 100708153 | intron variant | C/T | snv | 0.53 | 4 | ||||
rs59228823 | 14 | 100718850 | regulatory region variant | G/C | snv | 0.29 | 1 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs6590816 | 11 | 100730902 | intron variant | G/A | snv | 0.40 | 4 | ||||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
rs486023 | 11 | 100772406 | intron variant | G/A | snv | 0.25 | 2 | ||||
rs10883543 | 10 | 100792995 | intron variant | G/T | snv | 0.91 | 1 | ||||
rs4551692 | 10 | 100796696 | intron variant | G/A | snv | 0.91 | 2 | ||||
rs112184198 | 10 | 100844757 | intergenic variant | G/A | snv | 9.3E-02 | 1 | ||||
rs10895025 | 11 | 100877772 | intron variant | T/C | snv | 0.63 | 1 | ||||
rs10883617 | 10 | 101353278 | upstream gene variant | T/C | snv | 0.28 | 1 | ||||
rs17248480 | 4 | 101514108 | intron variant | G/A | snv | 1.8E-02 | 2 | ||||
rs142449193 | 8 | 101738369 | intron variant | C/T | snv | 6.9E-02 | 1 | ||||
rs3218248 | 10 | 101768487 | downstream gene variant | G/A | snv | 1.4E-02 | 1 | ||||
rs10409243 | 19 | 10222312 | 3 prime UTR variant | C/A;G;T | snv | 6 | |||||
rs2116942 | 19 | 10223987 | missense variant | T/A;G | snv | 3.5E-04; 0.54 | 1 |