Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17115149 | 0.882 | 0.160 | 10 | 102837961 | upstream gene variant | G/A;T | snv | 4 | |||
rs2296147 | 0.695 | 0.280 | 13 | 102846025 | 5 prime UTR variant | T/C | snv | 0.38 | 21 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs1799796 | 0.790 | 0.240 | 14 | 103699590 | intron variant | T/A;C | snv | 0.31 | 7 | ||
rs141752671 | 0.708 | 0.280 | 11 | 103745837 | intron variant | A/G | snv | 5.4E-03 | 17 | ||
rs148883465 | 0.708 | 0.280 | 11 | 103813371 | intron variant | A/G | snv | 7.2E-03 | 17 | ||
rs200182588 | 0.827 | 0.160 | 9 | 104094409 | 5 prime UTR variant | -/GC | ins | 7.0E-06 | 6 | ||
rs156113 | 0.925 | 0.080 | 6 | 104369868 | intergenic variant | A/T | snv | 0.96 | 2 | ||
rs2494732 | 0.763 | 0.240 | 14 | 104772855 | intron variant | T/C | snv | 0.50 | 0.47 | 11 | |
rs3730358 | 0.724 | 0.360 | 14 | 104780070 | intron variant | G/A;C | snv | 0.16; 4.0E-03 | 14 | ||
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs636291 | 0.925 | 0.080 | 1 | 10496040 | intron variant | G/A | snv | 0.55 | 2 | ||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 28 | ||
rs1221877686 | 0.925 | 0.080 | 4 | 105234193 | missense variant | G/A | snv | 2 | |||
rs9287719 | 1.000 | 0.080 | 2 | 10570604 | downstream gene variant | C/T | snv | 0.60 | 1 | ||
rs12315175 | 0.925 | 0.080 | 12 | 107105494 | intron variant | T/C | snv | 0.18 | 2 | ||
rs1283104 | 1.000 | 0.080 | 3 | 107243674 | intron variant | C/G | snv | 0.43 | 1 | ||
rs817826 | 0.925 | 0.080 | 9 | 107394019 | intergenic variant | C/T | snv | 0.81 | 2 | ||
rs4988483 | 0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 | 11 | |
rs2237706 | 1.000 | 0.080 | 7 | 107992726 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
rs197056 | 0.925 | 0.080 | 16 | 1081695 | upstream gene variant | A/C;G | snv | 2 | |||
rs197057 | 0.925 | 0.080 | 16 | 1082015 | upstream gene variant | C/G | snv | 0.53 | 2 |