Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10025419 | 4 | 100647799 | intron variant | G/A | snv | 0.87 | 1 | ||||
rs10041590 | 5 | 24064827 | intron variant | T/C;G | snv | 2 | |||||
rs10054178 | 5 | 24059742 | intron variant | A/G | snv | 7.5E-02 | 2 | ||||
rs10056373 | 5 | 24069684 | intron variant | C/T | snv | 7.4E-02 | 2 | ||||
rs10119043 | 9 | 135122706 | downstream gene variant | C/T | snv | 0.11 | 2 | ||||
rs1015164 | 0.925 | 3 | 46410189 | intron variant | A/C;G;T | snv | 8 | ||||
rs10178992 | 2 | 233749231 | intron variant | T/A | snv | 0.37 | 4 | ||||
rs10179091 | 2 | 233749337 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 11 | ||
rs10827209 | 10 | 33198261 | intron variant | A/C | snv | 0.23 | 2 | ||||
rs10892961 | 11 | 123093392 | intron variant | A/C;G;T | snv | 2 | |||||
rs10929301 | 2 | 233755003 | splice region variant | C/G;T | snv | 0.48 | 4 | ||||
rs10929302 | 2 | 233757136 | intron variant | G/A | snv | 0.30 | 4 | ||||
rs11011237 | 10 | 37531016 | intron variant | G/A | snv | 9.2E-02 | 2 | ||||
rs11012476 | 0.925 | 0.120 | 10 | 21003994 | intron variant | C/T | snv | 3.5E-02 | 3 | ||
rs11087114 | 20 | 14931037 | intron variant | G/A;C | snv | 1 | |||||
rs11218976 | 11 | 123090950 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs11228672 | 11 | 56597931 | non coding transcript exon variant | G/A;C | snv | 2 | |||||
rs113051092 | 5 | 24060490 | intron variant | A/T | snv | 7.4E-02 | 2 | ||||
rs113162402 | 17 | 58522103 | splice acceptor variant | T/A | snv | 1 | |||||
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs11568350 | 0.790 | 0.240 | 2 | 189565370 | missense variant | C/A | snv | 3.8E-03 | 1.6E-02 | 9 | |
rs11673726 | 2 | 233755414 | non coding transcript exon variant | G/A;T | snv | 4 | |||||
rs11695484 | 2 | 233745803 | intron variant | A/G | snv | 0.30 | 3 |