Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 23 | ||
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 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs6584283 | 0.776 | 0.080 | 10 | 99530544 | intron variant | T/C | snv | 0.56 | 12 | ||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 11 | |||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs76428106 | 0.851 | 0.040 | 13 | 28029870 | intron variant | T/C;G | snv | 10 | |||
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs445 | 7 | 92779056 | intron variant | C/T | snv | 0.14 | 9 | ||||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 8 | |||
rs12266014 | 10 | 24922362 | intron variant | C/T | snv | 0.26 | 7 | ||||
rs2038700 | 14 | 24992783 | intron variant | T/C | snv | 0.53 | 7 | ||||
rs333947 | 1 | 109928142 | intron variant | G/A | snv | 0.13 | 7 | ||||
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 7 | ||||
rs13063578 | 3 | 47046347 | intron variant | T/A | snv | 0.46 | 5 | ||||
rs11327184 | 8 | 129592027 | intron variant | C/- | delins | 0.40 | 4 | ||||
rs12711490 | 0.925 | 0.080 | 16 | 85939422 | intron variant | T/C | snv | 0.18 | 4 | ||
rs13277237 | 8 | 129592317 | intron variant | G/A | snv | 0.53 | 4 | ||||
rs1700159 | 1.000 | 0.040 | 12 | 51912002 | intron variant | C/A;G;T | snv | 4 |