Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 7 | ||||
rs3747207 | 22 | 43928975 | intron variant | G/A | snv | 0.22 | 7 | ||||
rs9376090 | 6 | 135090090 | intron variant | T/C | snv | 0.19 | 7 | ||||
rs10761731 | 10 | 63267850 | intron variant | A/T | snv | 0.38 | 6 | ||||
rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 | ||||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 5 | |||||
rs142550358 | 9 | 88777772 | intron variant | CT/- | delins | 3.9E-02 | 5 | ||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 5 | ||||
rs192022 | 11 | 108378047 | intron variant | C/G;T | snv | 5 | |||||
rs2068888 | 10 | 93079885 | downstream gene variant | G/A | snv | 0.42 | 5 |