Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs367597251 | 0.807 | 0.080 | 12 | 68839587 | missense variant | A/G | snv | 1.5E-04 | 5.1E-04 | 10 | |
rs1051861187 | 0.827 | 0.080 | 7 | 87409385 | missense variant | A/G | snv | 6 | |||
rs1760893 | 0.807 | 0.080 | 14 | 20412501 | intron variant | C/A | snv | 0.89 | 6 | ||
rs2299939 | 0.827 | 0.080 | 10 | 87897393 | intron variant | C/A;T | snv | 5 | |||
rs5854292 | 0.851 | 0.080 | 3 | 168680960 | intron variant | AA/-;A;AAA | delins | 5 | |||
rs1234220 | 0.851 | 0.080 | 10 | 87885716 | intron variant | A/G | snv | 9.1E-02 | 4 | ||
rs1330010954 | 0.882 | 0.080 | 8 | 13094897 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
rs230525 | 0.882 | 0.080 | 4 | 102537720 | non coding transcript exon variant | G/A | snv | 0.69 | 4 | ||
rs230530 | 0.882 | 0.080 | 4 | 102532823 | intron variant | A/G | snv | 0.37 | 4 | ||
rs372894000 | 0.882 | 0.080 | 8 | 13092766 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 4 | |
rs756966085 | 0.882 | 0.080 | 8 | 13090431 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 4 | |
rs80309960 | 0.851 | 0.080 | 2 | 216122110 | missense variant | T/A | snv | 3.5E-04 | 1.1E-03 | 4 | |
rs12732894 | 0.882 | 0.080 | 1 | 17582733 | intron variant | G/A | snv | 1.6E-02 | 3 | ||
rs1476081557 | 0.882 | 0.080 | 19 | 35721455 | missense variant | G/T | snv | 7.0E-06 | 3 | ||
rs2244444 | 0.882 | 0.080 | 1 | 17520426 | intergenic variant | C/T | snv | 0.55 | 3 | ||
rs230496 | 0.882 | 0.080 | 4 | 102567334 | intron variant | G/A | snv | 0.59 | 3 | ||
rs3811741 | 0.882 | 0.080 | 4 | 127882004 | intron variant | G/A | snv | 0.74 | 3 | ||
rs587782237 | 0.882 | 0.080 | 17 | 7670637 | missense variant | C/T | snv | 3 | |||
rs745501336 | 0.882 | 0.080 | 3 | 129091263 | missense variant | C/T | snv | 4.6E-05 | 7.0E-06 | 3 | |
rs764555290 | 0.882 | 0.080 | 12 | 52492759 | missense variant | G/C | snv | 1.2E-05 | 1.4E-05 | 3 | |
rs779555087 | 0.882 | 0.080 | 20 | 44414561 | missense variant | A/G | snv | 1.6E-05 | 1.4E-05 | 3 | |
rs1302103336 | 0.776 | 0.120 | 11 | 125637491 | missense variant | T/C | snv | 8.1E-06 | 12 | ||
rs4024 | 0.827 | 0.120 | 4 | 73435667 | intron variant | G/A | snv | 0.52 | 7 | ||
rs737241 | 0.827 | 0.120 | 4 | 73451012 | intron variant | G/A;C | snv | 7 | |||
rs867384693 | 0.851 | 0.120 | 5 | 141625349 | missense variant | C/A;T | snv | 6 |