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 | |||||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 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 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 11 | ||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 10 | ||
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs11066301 | 0.827 | 0.200 | 12 | 112433568 | intron variant | A/G | snv | 0.30 | 7 | ||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 7 | ||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 5 | |||||
rs11627485 | 14 | 65020976 | intron variant | T/C | snv | 0.36 | 5 | ||||
rs13412535 | 2 | 224010157 | intron variant | G/A | snv | 0.17 | 5 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs7394579 | 1.000 | 0.080 | 11 | 61813978 | intron variant | A/G | snv | 0.22 | 5 | ||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs7896518 | 10 | 63344740 | intron variant | A/G | snv | 0.38 | 4 | ||||
rs10761741 | 1.000 | 0.040 | 10 | 63306426 | intron variant | G/T | snv | 0.38 | 3 | ||
rs10886430 | 10 | 119250744 | intron variant | A/G | snv | 8.8E-02 | 3 | ||||
rs11071720 | 15 | 63049797 | intron variant | T/C;G | snv | 3 |