Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 11 | ||||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 10 | |||||
rs2954031 | 8 | 125479491 | intron variant | G/T | snv | 0.42 | 9 | ||||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 9 | ||||
rs9942416 | 5 | 75741470 | intergenic variant | C/G | snv | 0.53 | 9 | ||||
rs12721046 | 19 | 44917997 | intron variant | G/A | snv | 0.11 | 8 | ||||
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 8 | ||||
rs740746 | 10 | 114033028 | intergenic variant | G/A | snv | 0.70 | 8 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 7 | ||||
rs112875651 | 8 | 125494452 | intron variant | G/A | snv | 0.31 | 7 | ||||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 7 | ||||
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 7 | ||||
rs11570255 | 1.000 | 20 | 59300861 | missense variant | G/A;T | snv | 3.3E-03; 2.9E-05 | 7 | |||
rs115849089 | 8 | 20054859 | intergenic variant | G/A | snv | 9.8E-02 | 7 | ||||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 7 | ||||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
rs174529 | 11 | 61776489 | intron variant | T/C | snv | 0.34 | 7 | ||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 7 | ||||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 7 | ||||
rs6982636 | 8 | 125467073 | intron variant | G/A | snv | 0.43 | 7 | ||||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 7 | ||||
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 7 |