Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1283377907 | 1.000 | 0.120 | 16 | 88842829 | missense variant | T/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs1288687291 | 1.000 | 0.120 | 16 | 88843167 | synonymous variant | T/C | snv | 7.4E-06 | 1 | ||
rs1296755011 | 1.000 | 0.120 | 16 | 88842799 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1301146300 | 1.000 | 0.120 | 16 | 88837721 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
rs1301198698 | 1.000 | 0.120 | 16 | 88837690 | missense variant | G/C | snv | 1 | |||
rs1303492021 | 1.000 | 0.120 | 16 | 88814510 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1308500116 | 1.000 | 0.120 | 16 | 88837722 | missense variant | A/G | snv | 1.2E-05 | 1 | ||
rs1401175486 | 1.000 | 0.120 | 16 | 88818009 | missense variant | T/A;C | snv | 1 | |||
rs141340188 | 1.000 | 0.120 | 16 | 88841965 | missense variant | G/A;T | snv | 8.2E-06 | 1 | ||
rs1421990673 | 1.000 | 0.120 | 16 | 88842792 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1444754604 | 1.000 | 0.120 | 16 | 88841068 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs145798311 | 1.000 | 0.120 | 16 | 88842769 | missense variant | G/A | snv | 4.0E-05 | 4.2E-05 | 1 | |
rs146093755 | 1.000 | 0.120 | 16 | 88840999 | missense variant | C/T | snv | 8.0E-06 | 3.5E-05 | 1 | |
rs150734270 | 1.000 | 0.120 | 16 | 88826714 | missense variant | C/T | snv | 1.8E-03 | 1.7E-03 | 1 | |
rs1567526805 | 1.000 | 0.120 | 16 | 88832000 | stop gained | G/A | snv | 1 | |||
rs1567538216 | 1.000 | 0.120 | 16 | 88842831 | splice acceptor variant | T/C | snv | 1 | |||
rs191519947 | 1.000 | 0.120 | 16 | 88842807 | missense variant | A/C;G | snv | 4.8E-05; 3.3E-04 | 1 | ||
rs199638097 | 1.000 | 0.120 | 16 | 88842811 | missense variant | C/T | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs200374326 | 1.000 | 0.120 | 16 | 88841083 | stop gained | G/A | snv | 1.6E-05 | 2.8E-05 | 1 | |
rs267606838 | 1.000 | 0.120 | 16 | 88826822 | missense variant | C/T | snv | 1 | |||
rs398123433 | 1.000 | 0.120 | 16 | 88814488 | missense variant | C/A | snv | 1.4E-05 | 1 | ||
rs398123438 | 1.000 | 0.120 | 16 | 88837725 | missense variant | C/T | snv | 2.8E-05 | 2.1E-05 | 1 | |
rs398123439 | 1.000 | 0.120 | 16 | 88837711 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs398123440 | 1.000 | 0.120 | 16 | 88835779 | missense variant | G/A;T | snv | 2.0E-05; 4.0E-06 | 1 | ||
rs537013895 | 1.000 | 0.120 | 16 | 88832048 | missense variant | T/A;C | snv | 7.6E-05 | 2.1E-05 | 1 |