Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 16 | ||
rs4246215 | 0.677 | 0.320 | 11 | 61796827 | 3 prime UTR variant | G/C;T | snv | 13 | |||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 11 | |
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 10 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs174549 | 0.851 | 0.240 | 11 | 61803910 | 5 prime UTR variant | G/A | snv | 0.26 | 8 | ||
rs174550 | 0.925 | 0.160 | 11 | 61804006 | 5 prime UTR variant | T/C | snv | 0.28 | 7 | ||
rs174601 | 0.925 | 0.080 | 11 | 61855668 | non coding transcript exon variant | C/A;T | snv | 7 | |||
rs174545 | 1.000 | 0.080 | 11 | 61801834 | 3 prime UTR variant | C/A;G | snv | 0.28 | 4 | ||
rs174541 | 1.000 | 0.080 | 11 | 61798436 | intron variant | T/C | snv | 0.29 | 4 | ||
rs2880301 | 1.000 | 0.040 | 13 | 19526394 | intron variant | C/T | snv | 3 | |||
rs12623456 | 2 | 163162632 | intergenic variant | T/C | snv | 2.2E-02 | 2 | ||||
rs17254590 | 13 | 106384996 | downstream gene variant | G/C | snv | 2.8E-02 | 2 | ||||
rs2581624 | 3 | 142915027 | intron variant | G/C;T | snv | 0.29 | 2 | ||||
rs3762220 | 20 | 18797336 | upstream gene variant | G/A;T | snv | 2 | |||||
rs62519907 | 8 | 71696834 | intron variant | G/A;T | snv | 0.17 | 2 | ||||
rs7160151 | 14 | 49336446 | intergenic variant | A/G;T | snv | 2 | |||||
rs77164426 | 2 | 146756888 | intergenic variant | A/G | snv | 1.8E-02 | 2 | ||||
rs16838623 | 1 | 239648090 | intron variant | A/C | snv | 3.4E-02 | 2 | ||||
rs113847670 | 10 | 127076415 | intron variant | C/T | snv | 3.3E-02 | 2 | ||||
rs13431652 | 0.925 | 0.080 | 2 | 168896905 | intron variant | T/C | snv | 0.24 | 2 | ||
rs10414689 | 19 | 51293045 | regulatory region variant | T/C | snv | 0.11 | 1 | ||||
rs10518202 | 4 | 78758523 | intergenic variant | G/T | snv | 9.6E-02 | 1 | ||||
rs12529874 | 6 | 98014625 | intron variant | G/A | snv | 2.6E-02 | 1 |