Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 8 | ||
rs9277554 | 0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 | 5 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 4 | |||
rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 3 | ||
rs6933404 | 0.925 | 0.280 | 6 | 137638098 | intergenic variant | T/C | snv | 0.16 | 2 | ||
rs4282438 | 0.807 | 0.280 | 6 | 33104395 | intron variant | T/G | snv | 3.1E-02 | 2 | ||
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 2 | ||
rs5029939 | 0.701 | 0.440 | 6 | 137874586 | intron variant | C/G | snv | 0.13 | 2 | ||
rs11209032 | 0.752 | 0.400 | 1 | 67274409 | upstream gene variant | G/A | snv | 0.30 | 1 | ||
rs359457 | 0.925 | 0.240 | 5 | 173852839 | intergenic variant | C/T | snv | 0.59 | 1 | ||
rs9271588 | 0.925 | 0.200 | 6 | 32623176 | TF binding site variant | T/C | snv | 0.43 | 1 | ||
rs2736345 | 0.882 | 0.280 | 8 | 11494976 | intron variant | A/G | snv | 0.35 | 1 | ||
rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 1 | ||
rs11805303 | 0.827 | 0.240 | 1 | 67209833 | intron variant | C/T | snv | 0.30 | 1 | ||
rs3135394 | 0.851 | 0.240 | 6 | 32440720 | intron variant | A/G | snv | 6.3E-02 | 1 | ||
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 1 | ||
rs3757387 | 0.851 | 0.280 | 7 | 128936032 | upstream gene variant | T/C | snv | 0.38 | 1 | ||
rs3823536 | 0.925 | 0.280 | 7 | 128939612 | intron variant | G/A | snv | 0.40 | 1 | ||
rs117026326 | 0.752 | 0.440 | 7 | 74711703 | intron variant | C/T | snv | 1.3E-02 | 1 | ||
rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 1 | ||
rs11889341 | 0.732 | 0.480 | 2 | 191079016 | intron variant | C/T | snv | 0.21 | 1 | ||
rs2230926 | 0.662 | 0.440 | 6 | 137874929 | missense variant | T/C;G | snv | 4.0E-06; 5.4E-02 | 1 |