Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs187084 | 0.641 | 0.480 | 3 | 52227015 | intron variant | A/G | snv | 0.38 | 36 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs12598357 | 0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 | 15 | ||
rs12928404 | 0.724 | 0.240 | 16 | 28835925 | splice region variant | T/C | snv | 0.44 | 0.45 | 15 | |
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs17518584 | 0.827 | 0.160 | 3 | 85555773 | intron variant | C/T | snv | 0.50 | 8 | ||
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 7 | ||||
rs2239647 | 0.851 | 0.080 | 14 | 32823537 | synonymous variant | A/C | snv | 0.60 | 0.65 | 7 | |
rs35789010 | 0.851 | 0.200 | 6 | 25513951 | intron variant | G/A | snv | 4.1E-02 | 7 | ||
rs2710323 | 0.851 | 0.080 | 3 | 52781889 | intron variant | T/C | snv | 0.49 | 0.54 | 7 | |
rs7531118 | 1.000 | 0.080 | 1 | 72371556 | intron variant | T/C | snv | 0.40 | 7 | ||
rs3817334 | 1.000 | 0.080 | 11 | 47629441 | intron variant | C/T | snv | 0.36 | 7 | ||
rs17650792 | 0.827 | 0.080 | 3 | 49352817 | downstream gene variant | A/G | snv | 0.42 | 6 | ||
rs7302200 | 0.851 | 0.200 | 12 | 56055651 | regulatory region variant | G/A | snv | 0.23 | 6 | ||
rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 6 | ||
rs2007044 | 0.882 | 0.040 | 12 | 2235794 | intron variant | A/G | snv | 0.50 | 6 | ||
rs3749034 | 0.827 | 0.040 | 2 | 170816965 | 5 prime UTR variant | G/A;T | snv | 6 | |||
rs2032447 | 0.925 | 0.120 | 6 | 26044141 | non coding transcript exon variant | A/G | snv | 4.1E-06; 0.67 | 0.67 | 6 | |
rs12938031 | 0.851 | 0.160 | 17 | 45777136 | intron variant | A/G | snv | 0.26 | 6 | ||
rs3101336 | 1.000 | 0.080 | 1 | 72285502 | intron variant | T/C | snv | 0.62 | 6 | ||
rs2071303 | 0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 | 6 | |
rs1541374 | 4 | 105127203 | intergenic variant | T/A;G | snv | 5 | |||||
rs2388334 | 0.882 | 0.040 | 6 | 98143746 | intron variant | A/G | snv | 0.39 | 5 | ||
rs35225200 | 1.000 | 0.040 | 4 | 102225731 | intergenic variant | A/C | snv | 5.4E-02 | 5 | ||
rs17522122 | 0.925 | 0.040 | 14 | 32833676 | 3 prime UTR variant | G/T | snv | 0.41 | 5 |