Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs12721046 | 19 | 44917997 | intron variant | G/A | snv | 0.11 | 8 | ||||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
rs11568746 | 9 | 99105926 | intron variant | C/G | snv | 2.1E-05 | 6 | ||||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs17240378 | 16 | 67942790 | intron variant | G/C;T | snv | 4.0E-06 | 6 | ||||
rs1874148 | 10 | 74114657 | intron variant | A/G | snv | 1.8E-02 | 6 | ||||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 | |||||
rs2230667 | 19 | 49662445 | missense variant | C/T | snv | 1.0E-04 | 1.4E-05 | 6 | |||
rs2980869 | 8 | 125476008 | intron variant | C/T | snv | 0.48 | 6 | ||||
rs2980875 | 8 | 125469505 | intron variant | A/C;G;T | snv | 6 | |||||
rs2980880 | 8 | 125468730 | intron variant | G/A | snv | 0.69 | 6 | ||||
rs3093267 | 13 | 113118661 | missense variant | G/A;T | snv | 8.0E-05 | 6 | ||||
rs33980385 | 19 | 40991388 | missense variant | A/G | snv | 6 | |||||
rs34090729 | 9 | 134401999 | non coding transcript exon variant | C/T | snv | 1.6E-04 | 3.6E-04 | 6 | |||
rs34183407 | 2 | 73454052 | missense variant | C/T | snv | 2.1E-05 | 3.5E-05 | 6 | |||
rs35381288 | 8 | 37965106 | non coding transcript exon variant | C/G | snv | 7.4E-03 | 6 | ||||
rs35980686 | 19 | 44757093 | missense variant | T/C | snv | 1.1E-03 | 4.4E-03 | 6 | |||
rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
rs4251583 | 12 | 43783705 | missense variant | A/G | snv | 8.6E-04 | 1.1E-03 | 6 | |||
rs5176 | 1 | 53246137 | 3 prime UTR variant | T/G | snv | 6.4E-04 | 6 | ||||
rs533617 | 2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 | 6 | |||
rs583104 | 1 | 109278685 | downstream gene variant | G/T | snv | 0.63 | 6 | ||||
rs6982636 | 8 | 125467073 | intron variant | G/A | snv | 0.43 | 6 | ||||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 6 |