Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11727676 | 0.776 | 0.080 | 4 | 144737912 | synonymous variant | T/C | snv | 6.6E-02 | 6.4E-02 | 14 | |
rs2070699 | 0.752 | 0.080 | 6 | 12292539 | intron variant | G/C;T | snv | 0.45 | 14 | ||
rs4925386 | 0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 | 14 | ||
rs12916300 | 0.742 | 0.080 | 15 | 28165345 | intron variant | C/T | snv | 0.50 | 13 | ||
rs58658771 | 0.776 | 0.080 | 15 | 32709533 | intergenic variant | T/A | snv | 0.20 | 13 | ||
rs7229639 | 0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 | 13 | ||
rs10821907 | 0.776 | 0.080 | 10 | 50888694 | upstream gene variant | C/T | snv | 0.20 | 12 | ||
rs4360494 | 0.776 | 0.080 | 1 | 37990219 | upstream gene variant | G/C | snv | 0.45 | 12 | ||
rs6058093 | 0.776 | 0.080 | 20 | 34625392 | intron variant | A/C | snv | 0.55 | 12 | ||
rs6584283 | 0.776 | 0.080 | 10 | 99530544 | intron variant | T/C | snv | 0.56 | 12 | ||
rs6691170 | 0.776 | 0.080 | 1 | 221872104 | intergenic variant | G/T | snv | 0.34 | 12 | ||
rs9470361 | 0.776 | 0.080 | 6 | 36655602 | regulatory region variant | G/A;T | snv | 12 | |||
rs11255841 | 0.776 | 0.080 | 10 | 8697617 | intergenic variant | T/A | snv | 0.25 | 11 | ||
rs11874392 | 0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 | 11 | ||
rs1412834 | 0.790 | 0.080 | 9 | 22110132 | intron variant | T/C | snv | 0.64 | 11 | ||
rs2179593 | 0.790 | 0.080 | 20 | 44031646 | intron variant | C/A | snv | 0.71 | 11 | ||
rs35107139 | 0.776 | 0.080 | 14 | 53952388 | intron variant | A/C;G;T | snv | 11 | |||
rs35446936 | 0.776 | 0.080 | 3 | 169768720 | intron variant | G/A | snv | 0.21 | 11 | ||
rs4813802 | 0.776 | 0.080 | 20 | 6718948 | regulatory region variant | T/G | snv | 0.28 | 11 | ||
rs56848936 | 0.776 | 0.080 | 19 | 45818249 | intron variant | A/G | snv | 1.9E-02 | 11 | ||
rs6063514 | 0.776 | 0.080 | 20 | 50438781 | intergenic variant | C/T | snv | 0.42 | 11 | ||
rs10049390 | 0.776 | 0.080 | 3 | 133982275 | intron variant | G/A | snv | 0.67 | 10 | ||
rs10457678 | 0.790 | 0.080 | 6 | 138801103 | intron variant | A/G | snv | 0.19 | 10 | ||
rs10511330 | 0.776 | 0.080 | 3 | 114402172 | intron variant | T/C | snv | 0.22 | 10 | ||
rs1078643 | 0.776 | 0.080 | 17 | 10803924 | missense variant | G/A;C | snv | 10 |