Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893875 | 0.742 | 0.120 | 4 | 89828170 | missense variant | C/T | snv | 4.0E-06 | 13 | ||
rs242557 | 0.752 | 0.200 | 17 | 45942346 | intron variant | G/A | snv | 0.36 | 12 | ||
rs121909330 | 0.752 | 0.200 | 9 | 35065364 | missense variant | G/A;C;T | snv | 11 | |||
rs121909334 | 0.752 | 0.200 | 9 | 35065255 | missense variant | C/T | snv | 1.6E-05 | 10 | ||
rs767543900 | 0.790 | 0.120 | 17 | 45971879 | missense variant | A/C;G | snv | 4.0E-06 | 10 | ||
rs11931074 | 0.851 | 0.080 | 4 | 89718364 | intron variant | G/A;C;T | snv | 7 | |||
rs201106962 | 0.851 | 0.080 | 4 | 89828156 | missense variant | A/C | snv | 8.0E-05 | 7.0E-05 | 5 | |
rs2306604 | 0.827 | 0.080 | 10 | 58388932 | intron variant | A/C;G;T | snv | 5 | |||
rs3764435 | 0.827 | 0.120 | 9 | 72901960 | intron variant | A/C;T | snv | 5 | |||
rs1801474 | 0.851 | 0.080 | 6 | 162201165 | missense variant | C/T | snv | 7.1E-02 | 5.3E-02 | 4 | |
rs2281983 | 0.851 | 0.080 | 10 | 102231624 | missense variant | G/A;C;T | snv | 0.62; 8.3E-06 | 4 | ||
rs6347 | 0.851 | 0.080 | 5 | 1411297 | synonymous variant | T/C | snv | 0.23 | 0.32 | 4 | |
rs2420616 | 0.882 | 0.080 | 10 | 119316984 | intron variant | A/G | snv | 0.69 | 3 | ||
rs4752293 | 0.882 | 0.080 | 10 | 119342186 | intron variant | C/T | snv | 0.74 | 3 | ||
rs8126696 | 0.882 | 0.080 | 21 | 37358422 | intron variant | T/C | snv | 0.64 | 3 |