Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs987763 | 6 | 126960402 | intron variant | C/A;T | snv | 1 | |||||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 12 | ||
rs2229616 | 0.732 | 0.200 | 18 | 60372043 | missense variant | C/T | snv | 1.6E-02 | 1.6E-02 | 2 | |
rs7797307 | 7 | 69221140 | intron variant | G/C | snv | 7.6E-02 | 1 | ||||
rs12731740 | 1 | 207851475 | intron variant | C/T | snv | 9.1E-02 | 1 | ||||
rs6931262 | 6 | 7217284 | non coding transcript exon variant | C/T | snv | 0.10 | 1 | ||||
rs2278426 | 1.000 | 0.080 | 19 | 11239812 | missense variant | C/T | snv | 0.11 | 0.11 | 2 | |
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 20 | |
rs2235529 | 1.000 | 0.040 | 1 | 22123994 | intron variant | C/T | snv | 0.13 | 1 | ||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 1 | |||
rs1876829 | 1.000 | 0.040 | 17 | 45834077 | intron variant | T/C | snv | 0.15 | 0.14 | 2 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 4 | |
rs1051921 | 0.925 | 0.120 | 7 | 73593613 | 3 prime UTR variant | G/A | snv | 0.15 | 6 | ||
rs17249754 | 0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 | 3 | ||
rs1055144 | 1.000 | 0.040 | 7 | 25831489 | non coding transcript exon variant | C/T | snv | 0.16 | 2 | ||
rs55747707 | 7 | 73623036 | intron variant | G/A | snv | 0.16 | 1 | ||||
rs2287019 | 1.000 | 0.080 | 19 | 45698914 | intron variant | C/T | snv | 0.17 | 0.16 | 2 | |
rs987237 | 0.925 | 0.120 | 6 | 50835337 | intron variant | A/G | snv | 0.17 | 3 | ||
rs10019888 | 4 | 26061368 | regulatory region variant | A/G | snv | 0.17 | 2 | ||||
rs1800437 | 0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 | 1 | |
rs3088050 | 5 | 177299634 | 3 prime UTR variant | G/A | snv | 0.18 | 1 | ||||
rs8070723 | 0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 | 5 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 15 | ||
rs9750952 | 1.000 | 0.080 | 2 | 238827723 | intergenic variant | C/T | snv | 0.19 | 1 | ||
rs12714415 | 2 | 651430 | intergenic variant | T/C | snv | 0.19 | 2 |