Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 6 | |||||
rs760242 | 11 | 71435530 | missense variant | C/T | snv | 2.2E-04 | 6.3E-05 | 6 | |||
rs7993724 | 13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 | 6 | ||||
rs8138057 | 22 | 37665537 | intron variant | G/A | snv | 3.0E-03 | 1.3E-02 | 6 | |||
rs9341023 | 6 | 152062578 | intron variant | C/T | snv | 6 | |||||
rs9622186 | 22 | 35377961 | upstream gene variant | A/G | snv | 3.7E-03 | 6 | ||||
rs10478730 | 6 | 12297276 | downstream gene variant | C/T | snv | 1.2E-02 | 5 | ||||
rs11076175 | 16 | 56972466 | intron variant | A/G | snv | 0.20 | 5 | ||||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 5 | ||||
rs11828157 | 11 | 102947395 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs11921179 | 3 | 129976195 | intron variant | G/A | snv | 0.96 | 5 | ||||
rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 5 | ||||
rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
rs16880248 | 6 | 88141968 | 3 prime UTR variant | G/T | snv | 2.7E-02 | 5 | ||||
rs17243641 | 9 | 136886986 | intron variant | G/T | snv | 2.6E-03 | 5 | ||||
rs17513478 | 6 | 3101321 | intron variant | G/A | snv | 5.7E-03 | 5 | ||||
rs180327 | 11 | 116752943 | intron variant | C/T | snv | 0.58 | 5 | ||||
rs2072560 | 11 | 116791110 | missense variant | T/C | snv | 0.89 | 0.94 | 5 | |||
rs261336 | 15 | 58450219 | intron variant | G/A | snv | 0.81 | 5 | ||||
rs261338 | 15 | 58442806 | intron variant | A/G | snv | 0.83 | 5 | ||||
rs261342 | 15 | 58438954 | intron variant | G/A;C;T | snv | 5 | |||||
rs289714 | 16 | 56973539 | intron variant | G/A | snv | 0.76; 4.0E-06 | 0.70 | 5 | |||
rs34660894 | 12 | 57129111 | intron variant | G/A | snv | 2.3E-03 | 1.0E-02 | 5 | |||
rs35738419 | 9 | 134411944 | intron variant | C/T | snv | 7.3E-04 | 5 |