Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
rs385893 | 0.925 | 0.080 | 9 | 4763176 | downstream gene variant | T/C | snv | 0.44 | 6 | ||
rs7896518 | 10 | 63344740 | intron variant | A/G | snv | 0.38 | 4 | ||||
rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 13 | ||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs192022 | 11 | 108378047 | intron variant | C/G;T | snv | 5 | |||||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 19 | ||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs66505542 | 11 | 116752498 | intron variant | AA/-;A;AAA | delins | 5 |