Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 25 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 21 | |
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs174533 | 0.763 | 0.160 | 11 | 61781553 | intron variant | G/A | snv | 0.37 | 0.29 | 17 | |
rs10936599 | 0.637 | 0.600 | 3 | 169774313 | synonymous variant | C/T | snv | 0.29 | 0.21 | 15 | |
rs11727676 | 0.776 | 0.080 | 4 | 144737912 | synonymous variant | T/C | snv | 6.6E-02 | 6.4E-02 | 14 | |
rs174537 | 0.708 | 0.400 | 11 | 61785208 | non coding transcript exon variant | G/T | snv | 0.28 | 14 | ||
rs58658771 | 0.776 | 0.080 | 15 | 32709533 | intergenic variant | T/A | snv | 0.20 | 13 | ||
rs10821907 | 0.776 | 0.080 | 10 | 50888694 | upstream gene variant | C/T | snv | 0.20 | 12 | ||
rs9470361 | 0.776 | 0.080 | 6 | 36655602 | regulatory region variant | G/A;T | snv | 12 | |||
rs4759277 | 0.752 | 0.160 | 12 | 57139907 | intron variant | C/A | snv | 0.38 | 12 | ||
rs6058093 | 0.776 | 0.080 | 20 | 34625392 | intron variant | A/C | snv | 0.55 | 12 | ||
rs4360494 | 0.776 | 0.080 | 1 | 37990219 | upstream gene variant | G/C | snv | 0.45 | 12 | ||
rs6063514 | 0.776 | 0.080 | 20 | 50438781 | intergenic variant | C/T | snv | 0.42 | 11 | ||
rs35107139 | 0.776 | 0.080 | 14 | 53952388 | intron variant | A/C;G;T | snv | 11 | |||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 11 | ||
rs1537372 | 0.752 | 0.120 | 9 | 22103184 | intron variant | G/A;T | snv | 11 | |||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 11 | ||
rs2738783 | 0.763 | 0.160 | 20 | 63677259 | intron variant | T/G | snv | 0.85 | 11 | ||
rs11087784 | 0.776 | 0.080 | 20 | 7760329 | intergenic variant | A/G | snv | 0.13 | 10 | ||
rs11190164 | 0.776 | 0.080 | 10 | 99591947 | intergenic variant | A/G | snv | 0.19 | 10 | ||
rs11255841 | 0.776 | 0.080 | 10 | 8697617 | intergenic variant | T/A | snv | 0.25 | 10 | ||
rs11610543 | 0.776 | 0.080 | 12 | 42740389 | intergenic variant | A/G;T | snv | 10 | |||
rs116353863 | 0.776 | 0.080 | 6 | 31042408 | regulatory region variant | T/C | snv | 2.2E-02 | 10 | ||
rs12149163 | 0.776 | 0.080 | 16 | 86305709 | upstream gene variant | T/C | snv | 0.49 | 10 |