Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 14 | ||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 11 | |||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
rs11627485 | 14 | 65020976 | intron variant | T/C | snv | 0.36 | 5 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs17116384 | 11 | 114110519 | intron variant | A/G | snv | 0.25 | 3 | ||||
rs35150201 | 7 | 135661514 | upstream gene variant | T/G | snv | 0.42 | 3 | ||||
rs4499344 | 19 | 32582525 | intron variant | G/A | snv | 0.46 | 3 | ||||
rs2227831 | 5 | 76727669 | intron variant | A/G | snv | 2.7E-02 | 2 |