Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6471 | 0.683 | 0.360 | 6 | 32040110 | missense variant | G/A;C;T | snv | 1.2E-05; 5.3E-03 | 24 | ||
rs9378251 | 0.776 | 0.320 | 6 | 32038514 | missense variant | C/T | snv | 9.2E-05 | 5.4E-04 | 8 | |
rs6475 | 0.807 | 0.320 | 6 | 32039426 | missense variant | T/A | snv | 4.8E-04 | 1.2E-03 | 7 | |
rs7755898 | 0.827 | 0.240 | 6 | 32040421 | stop gained | C/T | snv | 3.6E-03 | 5 | ||
rs1030467767 | 0.882 | 0.200 | 6 | 32038538 | missense variant | A/C;T | snv | 8.6E-06 | 3 | ||
rs151344505 | 0.882 | 0.240 | 6 | 32040179 | missense variant | G/A | snv | 1.1E-04 | 9.8E-05 | 3 | |
rs267606757 | 0.882 | 0.200 | 6 | 32039162 | missense variant | A/C | snv | 3 | |||
rs547552654 | 0.882 | 0.200 | 6 | 32039165 | missense variant | A/C | snv | 3 | |||
rs550051210 | 0.882 | 0.200 | 6 | 32039118 | missense variant | C/A;T | snv | 7.0E-05 | 3 | ||
rs7769409 | 0.882 | 0.200 | 6 | 32040535 | missense variant | C/T | snv | 7.0E-05 | 3 | ||
rs9378252 | 0.882 | 0.200 | 6 | 32038610 | missense variant | A/G;T | snv | 4.4E-02 | 3 | ||
rs12530380 | 1.000 | 6 | 32039810 | missense variant | T/A | snv | 1.4E-05 | 1 | |||
rs6476 | 1.000 | 6 | 32039816 | missense variant | T/A;C | snv | 1.0E-03 | 1 | |||
rs749346869 | 1.000 | 6 | 32038498 | missense variant | C/T | snv | 1.4E-05 | 1 | |||
rs776989258 | 0.807 | 0.280 | 6 | 32041093 | missense variant | C/G;T | snv | 5.5E-04 | 6 | ||
rs200005406 | 0.851 | 0.200 | 6 | 32041097 | missense variant | G/A;C | snv | 8.8E-06; 3.3E-04 | 4 | ||
rs397509367 | 0.882 | 0.200 | 6 | 32041097 | frameshift variant | GG/C | delins | 3 | |||
rs768153689 | 1.000 | 10 | 122598858 | frameshift variant | G/- | delins | 1 | ||||
rs905880501 | 0.827 | 0.200 | 1 | 119422501 | stop gained | C/T | snv | 5 | |||
rs1801278 | 0.637 | 0.560 | 2 | 226795828 | missense variant | C/G;T | snv | 4.0E-06; 5.2E-02 | 38 | ||
rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
rs768768839 | 0.807 | 0.280 | 2 | 25161679 | missense variant | G/A | snv | 5.6E-06 | 6 | ||
rs1057868 | 0.763 | 0.320 | 7 | 75985688 | missense variant | C/T | snv | 0.31 | 0.27 | 9 | |
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs6445 | 0.827 | 0.240 | 6 | 32041006 | missense variant | C/T | snv | 4.6E-03 | 5.2E-03 | 5 |