Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 18 | |
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 16 | ||
rs11651755 | 0.763 | 0.160 | 17 | 37739849 | intron variant | T/C | snv | 0.52 | 4 | ||
rs183211 | 0.882 | 0.160 | 17 | 46710944 | intron variant | G/A | snv | 0.28 | 0.30 | 3 | |
rs7405776 | 0.807 | 0.120 | 17 | 37733029 | intron variant | G/A;C | snv | 3 | |||
rs8170 | 0.724 | 0.160 | 19 | 17278895 | synonymous variant | G/A | snv | 0.15 | 0.18 | 3 | |
rs10088218 | 0.851 | 0.120 | 8 | 128531703 | intron variant | G/A | snv | 0.13 | 2 | ||
rs11782652 | 0.851 | 0.120 | 8 | 81741409 | intron variant | A/G | snv | 6.6E-02 | 2 | ||
rs1243180 | 0.790 | 0.160 | 10 | 21626690 | intron variant | T/A | snv | 0.23 | 2 | ||
rs2072590 | 0.851 | 0.120 | 2 | 176177905 | non coding transcript exon variant | A/C;T | snv | 2 | |||
rs314276 | 0.807 | 0.280 | 6 | 104960124 | intron variant | A/C | snv | 0.65 | 2 | ||
rs3814113 | 0.827 | 0.200 | 9 | 16915023 | upstream gene variant | T/C | snv | 0.41 | 2 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 2 | |
rs757210 | 0.807 | 0.160 | 17 | 37736525 | intron variant | C/G;T | snv | 2 | |||
rs7651446 | 0.882 | 0.120 | 3 | 156689208 | intron variant | G/T | snv | 7.9E-02 | 2 | ||
rs9303542 | 0.882 | 0.120 | 17 | 48334138 | intron variant | A/G | snv | 0.34 | 2 | ||
rs10260419 | 0.882 | 0.120 | 7 | 11524758 | intron variant | C/G | snv | 0.26 | 1 | ||
rs11175194 | 0.925 | 0.120 | 12 | 63871057 | intron variant | G/A | snv | 0.15 | 1 | ||
rs115344852 | 1.000 | 0.120 | 6 | 28518321 | intron variant | A/C | snv | 1 | |||
rs1192691 | 0.925 | 0.120 | 10 | 36880367 | regulatory region variant | G/T | snv | 0.90 | 1 | ||
rs12039431 | 1.000 | 0.120 | 1 | 37616450 | intron variant | G/A | snv | 0.24 | 0.21 | 1 | |
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 1 | ||
rs1413299 | 0.925 | 0.120 | 9 | 98998959 | intron variant | G/A;T | snv | 1 | |||
rs142091544 | 0.925 | 0.120 | 5 | 168286995 | upstream gene variant | C/T | snv | 2.1E-02 | 1 | ||
rs1574560 | 1.000 | 0.120 | 3 | 166329716 | intergenic variant | T/C | snv | 0.42 | 1 |