Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6590811 | 11 | 100708153 | intron variant | C/T | snv | 0.53 | 4 | ||||
rs6590812 | 11 | 100711497 | intron variant | G/A | snv | 0.55 | 1 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs6590816 | 11 | 100730902 | intron variant | G/A | snv | 0.40 | 4 | ||||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
rs7801190 | 1.000 | 0.040 | 7 | 100860471 | non coding transcript exon variant | C/G | snv | 9.9E-02 | 2 | ||
rs10895068 | 0.752 | 0.240 | 11 | 101129483 | 5 prime UTR variant | C/T | snv | 3.6E-02 | 14 | ||
rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
rs104893831 | 0.925 | 0.040 | 3 | 10146549 | missense variant | G/A;C;T | snv | 2.0E-05 | 4 | ||
rs2228611 | 0.708 | 0.520 | 19 | 10156401 | synonymous variant | T/A;C | snv | 0.52 | 19 | ||
rs10860812 | 12 | 101894592 | intron variant | G/A | snv | 0.59 | 1 | ||||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs6219 | 1.000 | 0.080 | 12 | 102396414 | 3 prime UTR variant | C/T | snv | 8.9E-02 | 2 | ||
rs7136446 | 0.882 | 0.160 | 12 | 102444737 | intron variant | C/T | snv | 0.66 | 8 | ||
rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
rs11568818 | 0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv | 15 | |||
rs176185 | 10 | 102796297 | intron variant | G/C | snv | 0.82 | 1 | ||||
rs281432 | 0.851 | 0.280 | 19 | 10279982 | intron variant | C/G | snv | 0.52 | 12 | ||
rs104894145 | 0.925 | 0.240 | 10 | 102830946 | missense variant | G/A | snv | 3 | |||
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 | |
rs4919687 | 0.742 | 0.160 | 10 | 102835491 | non coding transcript exon variant | G/A | snv | 0.25 | 14 | ||
rs138009835 | 10 | 102839238 | intron variant | G/A;T | snv | 1 | |||||
rs13175330 | 5 | 102840757 | intron variant | A/G | snv | 7.8E-02 | 2 | ||||
rs679620 | 0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 | 17 |