Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1154556 | 1.000 | 0.040 | Y | 21979249 | intron variant | T/C | snv | 1 | |||
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs3027898 | 0.752 | 0.360 | X | 154010439 | downstream gene variant | C/A | snv | 11 | |||
rs3764880 | 0.752 | 0.320 | X | 12906707 | start lost | A/G | snv | 0.31 | 0.30 | 11 | |
rs3764879 | 0.807 | 0.320 | X | 12906578 | intron variant | C/G | snv | 0.30 | 6 | ||
rs3761581 | 0.851 | 0.160 | X | 129655744 | upstream gene variant | A/C | snv | 0.11 | 5 | ||
rs763802417 | 0.882 | 0.040 | X | 100862805 | missense variant | G/A | snv | 5.9E-06 | 5 | ||
rs2968915 | 1.000 | 0.040 | X | 40580182 | intron variant | G/A | snv | 3 | |||
rs56204867 | 0.925 | 0.040 | X | 129656490 | upstream gene variant | A/G | snv | 0.11 | 3 | ||
rs755559514 | 0.925 | 0.040 | X | 129648648 | missense variant | T/C;G | snv | 1.2E-05; 6.1E-06 | 3 | ||
rs3115758 | 1.000 | 0.040 | X | 129647887 | 3 prime UTR variant | C/A | snv | 0.21 | 0.31 | 1 | |
rs3115759 | 1.000 | 0.040 | X | 129647539 | 3 prime UTR variant | C/G;T | snv | 1 | |||
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs1232898090 | 0.637 | 0.600 | 22 | 46198429 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 40 | ||
rs4818 | 0.683 | 0.440 | 22 | 19963684 | synonymous variant | C/G;T | snv | 0.34 | 27 | ||
rs1801198 | 0.677 | 0.400 | 22 | 30615623 | missense variant | G/A;C | snv | 5.6E-05; 0.57 | 26 | ||
rs1065852 | 0.695 | 0.360 | 22 | 42130692 | missense variant | G/A | snv | 0.21 | 0.19 | 19 | |
rs2071746 | 0.708 | 0.320 | 22 | 35380679 | intron variant | A/T | snv | 0.49 | 18 | ||
rs749437638 | 0.752 | 0.240 | 22 | 19968597 | missense variant | C/T | snv | 2.4E-05 | 1.4E-05 | 14 | |
rs2096525 | 0.827 | 0.280 | 22 | 23894632 | non coding transcript exon variant | T/C | snv | 0.20 | 0.20 | 6 | |
rs1007888 | 0.882 | 0.120 | 22 | 23898914 | non coding transcript exon variant | C/T | snv | 0.46 | 4 | ||
rs8141797 | 0.882 | 0.120 | 22 | 24186073 | missense variant | A/G | snv | 8.1E-02 | 9.8E-02 | 3 | |
rs1081161 | 0.925 | 0.120 | 22 | 12200388 | intergenic variant | G/A | snv | 2 | |||
rs180803 | 0.925 | 0.080 | 22 | 24262890 | intron variant | G/A;T | snv | 2 | |||
rs6928 | 0.925 | 0.080 | 22 | 21760715 | 3 prime UTR variant | C/G | snv | 0.49 | 2 |