Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10444602 | 12 | 131708291 | upstream gene variant | T/G | snv | 0.51 | 1 | ||||
rs11659639 | 18 | 60500379 | intron variant | T/G | snv | 1.1E-02 | 1 | ||||
rs1173766 | 5 | 32804422 | intergenic variant | T/C | snv | 0.57 | 1 | ||||
rs11816631 | 10 | 97802815 | intergenic variant | A/G | snv | 8.8E-02 | 1 | ||||
rs12067906 | 1 | 192462868 | intron variant | T/C | snv | 0.12 | 1 | ||||
rs12098903 | 11 | 55899037 | downstream gene variant | A/T | snv | 5.7E-02 | 1 | ||||
rs12098904 | 11 | 55899077 | downstream gene variant | A/T | snv | 5.7E-02 | 1 | ||||
rs12098941 | 11 | 55898967 | downstream gene variant | T/A;G | snv | 1 | |||||
rs13002573 | 2 | 164058698 | intron variant | A/G | snv | 0.20 | 1 | ||||
rs13149993 | 4 | 80237391 | regulatory region variant | G/A;C | snv | 1 | |||||
rs13209747 | 6 | 126794309 | intron variant | C/G;T | snv | 0.36 | 1 | ||||
rs1384089 | 11 | 56081540 | upstream gene variant | G/C | snv | 6.0E-02 | 1 | ||||
rs1446468 | 2 | 164106976 | intron variant | T/C | snv | 0.40 | 1 | ||||
rs1492840 | 4 | 45764988 | intergenic variant | A/C;G;T | snv | 1 | |||||
rs16833934 | 3 | 164019462 | intergenic variant | A/G | snv | 0.34 | 1 | ||||
rs16849225 | 2 | 164050310 | intron variant | C/T | snv | 0.19 | 1 | ||||
rs16877320 | 6 | 15922795 | TF binding site variant | T/A;C | snv | 1 | |||||
rs17428471 | 7 | 27298248 | intergenic variant | G/T | snv | 9.4E-02 | 1 | ||||
rs17477177 | 1.000 | 0.080 | 7 | 106771412 | upstream gene variant | T/C | snv | 0.17 | 1 | ||
rs17510438 | 11 | 55902839 | downstream gene variant | G/A | snv | 5.7E-02 | 1 | ||||
rs17511107 | 11 | 55908549 | upstream gene variant | T/C | snv | 5.7E-02 | 1 | ||||
rs17512592 | 11 | 55922766 | intergenic variant | A/G | snv | 5.8E-02 | 1 | ||||
rs17530228 | 11 | 56081680 | upstream gene variant | A/G | snv | 6.0E-02 | 1 | ||||
rs17531933 | 11 | 56128173 | downstream gene variant | T/C;G | snv | 1 | |||||
rs17531954 | 11 | 56128255 | downstream gene variant | T/C | snv | 6.0E-02 | 1 |