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 | 6 | |||||
rs1018379423 | 1 | 22907986 | missense variant | G/T | snv | 4.0E-06 | 2.1E-05 | 4 | |||
rs140516819 | 7 | 55172999 | missense variant | A/C;G | snv | 4.0E-05 | 2.4E-04 | 4 | |||
rs1441008398 | 5 | 112839334 | missense variant | C/T | snv | 4.0E-06 | 4 | ||||
rs35918369 | 7 | 55205613 | missense variant | C/T | snv | 3.1E-04 | 3.3E-04 | 4 | |||
rs750605522 | 16 | 58722168 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 4 | |||
rs767136747 | 9 | 133717404 | missense variant | T/C | snv | 4.0E-06 | 4 | ||||
rs876660427 | 5 | 112838608 | missense variant | C/T | snv | 4 | |||||
rs10505476 | 8 | 127395871 | intron variant | C/T | snv | 0.38 | 3 | ||||
rs11121704 | 1 | 11233902 | intron variant | C/A;T | snv | 3 | |||||
rs1372047743 | 8 | 47960120 | missense variant | C/T | snv | 9.7E-06 | 3 | ||||
rs138105638 | 7 | 99766440 | stop gained | G/A;T | snv | 6.4E-05 | 7.7E-05 | 3 | |||
rs151227402 | 4 | 9783126 | missense variant | A/G | snv | 8.0E-05 | 3.1E-04 | 3 | |||
rs1639122 | 12 | 6601981 | missense variant | C/A;G | snv | 0.40 | 3 | ||||
rs16861205 | 3 | 186843845 | intron variant | G/A | snv | 0.14 | 3 | ||||
rs1800932 | 2 | 47790942 | synonymous variant | A/G | snv | 0.13 | 0.15 | 3 | |||
rs2071214 | 17 | 78223510 | missense variant | G/A | snv | 0.93 | 0.96 | 3 | |||
rs2294757 | 6 | 132713959 | missense variant | G/A | snv | 0.45 | 0.53 | 3 | |||
rs2970870 | 4 | 23891394 | intron variant | A/G | snv | 0.49 | 3 | ||||
rs3087468 | 16 | 2040233 | missense variant | C/A | snv | 3 | |||||
rs35697691 | 15 | 52061301 | missense variant | C/G | snv | 5.8E-02 | 5.9E-02 | 3 | |||
rs371217738 | 2 | 96115056 | missense variant | C/A;T | snv | 8.1E-06 | 3 | ||||
rs375526265 | 14 | 20457260 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 3 | |||
rs4524 | 1 | 169542517 | missense variant | T/C | snv | 0.28 | 0.24 | 3 | |||
rs4940177 | 18 | 52342374 | intron variant | T/C;G | snv | 3 |