Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs871656 | 0.827 | 0.120 | 2 | 102154822 | intron variant | T/A;C | snv | 5 | |||
rs3917265 | 1.000 | 0.120 | 2 | 102162001 | intron variant | T/C | snv | 0.50 | 2 | ||
rs13427957 | 1.000 | 0.080 | 2 | 102072571 | intron variant | C/T | snv | 0.46 | 1 | ||
rs4851541 | 2 | 102123999 | intron variant | G/T | snv | 0.40 | 1 | ||||
rs150946191 | 2 | 102116028 | intron variant | T/G | snv | 1.9E-02 | 1 | ||||
rs4141632 | 2 | 102140679 | intron variant | A/G;T | snv | 1 | |||||
rs9284725 | 2 | 102128394 | intron variant | C/A;T | snv | 0.82 | 1 | ||||
rs12712127 | 2 | 102110201 | intron variant | A/G | snv | 0.62 | 1 | ||||
rs1558643 | 2 | 102115231 | intron variant | T/C;G | snv | 1 | |||||
rs7588201 | 2 | 102129816 | intron variant | A/C | snv | 0.39 | 1 | ||||
rs2228139 | 2 | 102165189 | missense variant | C/A;G | snv | 5.6E-02 | 1 | ||||
rs3917254 | 2 | 102160058 | intron variant | G/A | snv | 0.16 | 1 |