Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs867114783 | 17 | 7675109 | missense variant | T/C | snv | 5 | |||||
rs1269252748 | 9 | 2641436 | missense variant | C/T | snv | 4 | |||||
rs760361706 | 22 | 46235326 | missense variant | G/C | snv | 4.0E-06 | 4 | ||||
rs9983925 | 21 | 45216929 | intron variant | C/T | snv | 0.46 | 4 | ||||
rs876660427 | 5 | 112838608 | missense variant | C/T | snv | 4 | |||||
rs140516819 | 7 | 55172999 | missense variant | A/C;G | snv | 4.0E-05 | 2.4E-04 | 4 | |||
rs35918369 | 7 | 55205613 | missense variant | C/T | snv | 3.1E-04 | 3.3E-04 | 4 | |||
rs1018379423 | 1 | 22907986 | missense variant | G/T | snv | 4.0E-06 | 2.1E-05 | 4 | |||
rs767136747 | 9 | 133717404 | missense variant | T/C | snv | 4.0E-06 | 4 | ||||
rs1441008398 | 5 | 112839334 | missense variant | C/T | snv | 4.0E-06 | 4 | ||||
rs750605522 | 16 | 58722168 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 4 | |||
rs863224683 | 17 | 7675224 | missense variant | G/A;C | snv | 4 | |||||
rs1057518011 | 1 | 1535766 | missense variant | C/T | snv | 4 | |||||
rs2640909 | 1 | 7830057 | missense variant | T/C | snv | 0.14 | 0.23 | 4 | |||
rs1052108705 | 6 | 31165217 | missense variant | C/T | snv | 4.1E-06 | 2.1E-05 | 3 | |||
rs768746587 | 6 | 31165136 | missense variant | C/T | snv | 8.4E-06 | 3 | ||||
rs755683317 | 21 | 10567746 | missense variant | G/A;C | snv | 2.4E-05 | 3 | ||||
rs778826879 | 16 | 30121948 | missense variant | C/G;T | snv | 1.2E-05; 8.0E-06 | 3 | ||||
rs10505476 | 8 | 127395871 | intron variant | C/T | snv | 0.38 | 3 | ||||
rs770684782 | 9 | 132288268 | stop gained | G/A | snv | 4.0E-06 | 3 | ||||
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 3 | ||||
rs1802710 | 14 | 100734308 | synonymous variant | T/A;C | snv | 0.63 | 3 | ||||
rs138105638 | 7 | 99766440 | stop gained | G/A;T | snv | 6.4E-05 | 7.7E-05 | 3 | |||
rs11121704 | 1 | 11233902 | intron variant | C/A;T | snv | 3 | |||||
rs375526265 | 14 | 20457260 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 3 |