Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1224426272 | 0.925 | 0.040 | 12 | 119869138 | missense variant | C/T | snv | 6 | |||
rs4409766 | 1.000 | 0.040 | 10 | 102856906 | intron variant | T/C | snv | 0.14 | 6 | ||
rs121917763 | 0.925 | 0.040 | 11 | 2167896 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 5 | |
rs4434553 | 1.000 | 0.040 | 7 | 100642568 | intron variant | A/G | snv | 0.40 | 5 | ||
rs45539432 | 0.851 | 0.040 | 1 | 20649109 | stop gained | C/T | snv | 4.0E-05 | 3.5E-05 | 5 | |
rs762472005 | 0.851 | 0.040 | 3 | 45722873 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 5 | |
rs763222239 | 0.827 | 0.040 | 3 | 184322862 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs1060499619 | 0.851 | 0.040 | 21 | 32681590 | missense variant | C/G | snv | 4 | |||
rs17563986 | 1.000 | 0.040 | 17 | 45913906 | intron variant | A/G | snv | 0.14 | 4 | ||
rs1801334 | 0.851 | 0.040 | 6 | 161360193 | missense variant | C/T | snv | 2.5E-02 | 2.5E-02 | 4 | |
rs1991556 | 1.000 | 0.040 | 17 | 46006036 | intron variant | G/A | snv | 0.14 | 4 | ||
rs368134308 | 0.882 | 0.040 | 6 | 162443356 | missense variant | C/A;G;T | snv | 3.2E-05; 2.6E-04 | 4 | ||
rs466448 | 0.925 | 0.040 | 21 | 26171790 | intron variant | A/C;G | snv | 4 | |||
rs71653619 | 1.000 | 0.040 | 1 | 7970934 | missense variant | G/A | snv | 7.9E-03 | 7.0E-03 | 4 | |
rs864309650 | 0.851 | 0.040 | 7 | 56104344 | missense variant | G/A | snv | 4 | |||
rs10518765 | 1.000 | 0.040 | 15 | 54388434 | intron variant | A/C | snv | 0.16 | 3 | ||
rs1060501198 | 0.925 | 0.040 | 17 | 7674900 | missense variant | T/C;G | snv | 3 | |||
rs12720208 | 0.925 | 0.040 | 8 | 16992890 | 3 prime UTR variant | G/A | snv | 5.5E-02 | 3 | ||
rs12817488 | 1.000 | 0.040 | 12 | 122811747 | intron variant | G/A | snv | 0.39 | 3 | ||
rs1290141855 | 1.000 | 0.040 | 16 | 55698539 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs1564282 | 1.000 | 0.040 | 4 | 858525 | intron variant | C/T | snv | 8.1E-02 | 3 | ||
rs1876829 | 1.000 | 0.040 | 17 | 45834077 | intron variant | T/C | snv | 0.15 | 0.14 | 3 | |
rs1981997 | 1.000 | 0.040 | 17 | 45979401 | non coding transcript exon variant | G/A | snv | 0.14 | 3 | ||
rs200660418 | 1.000 | 0.040 | 12 | 40310449 | missense variant | C/A;G;T | snv | 3 | |||
rs2668692 | 1.000 | 0.040 | 17 | 46215654 | intron variant | G/A;T | snv | 3 |