Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12130219 | 0.925 | 0.120 | 1 | 152189630 | non coding transcript exon variant | A/G | snv | 0.23 | 2 | ||
rs1384974 | 0.925 | 0.120 | 3 | 177009491 | downstream gene variant | T/C | snv | 9.6E-02 | 2 | ||
rs1528473 | 0.925 | 0.120 | 15 | 55094545 | downstream gene variant | A/G | snv | 7.6E-02 | 2 | ||
rs17728338 | 0.851 | 0.160 | 5 | 151098757 | downstream gene variant | G/A | snv | 7.1E-02 | 2 | ||
rs2059876 | 0.925 | 0.120 | 19 | 33639430 | intron variant | C/T | snv | 0.28 | 2 | ||
rs2533291 | 0.925 | 0.120 | 7 | 157712962 | intron variant | C/T | snv | 0.12 | 2 | ||
rs2944542 | 0.925 | 0.120 | 10 | 62610240 | intron variant | C/G | snv | 0.71 | 2 | ||
rs380743 | 0.925 | 0.120 | 19 | 48737757 | intron variant | G/A;C | snv | 2 | |||
rs4363385 | 0.925 | 0.120 | 1 | 153016845 | upstream gene variant | T/C | snv | 0.62 | 2 | ||
rs45616239 | 0.925 | 0.120 | 4 | 122335010 | intron variant | T/C | snv | 0.13 | 2 | ||
rs62176107 | 0.925 | 0.120 | 2 | 178436244 | missense variant | G/A;T | snv | 2 | |||
rs6548123 | 0.925 | 0.120 | 2 | 2221629 | intron variant | C/T | snv | 0.76 | 2 | ||
rs6596086 | 0.925 | 0.120 | 5 | 132616530 | intron variant | T/C | snv | 0.34 | 2 | ||
rs67766926 | 0.925 | 0.120 | 2 | 60936446 | downstream gene variant | C/G | snv | 0.17 | 2 | ||
rs73510898 | 0.925 | 0.120 | 19 | 10305768 | intron variant | G/A;C;T | snv | 2 | |||
rs80312298 | 0.925 | 0.120 | 10 | 129683009 | intron variant | C/A;T | snv | 2 | |||
rs9302874 | 0.925 | 0.120 | 17 | 78284479 | intergenic variant | C/T | snv | 0.24 | 2 | ||
rs9405490 | 0.925 | 0.120 | 6 | 1510423 | downstream gene variant | G/A | snv | 0.20 | 2 | ||
rs9952991 | 0.925 | 0.120 | 18 | 12780465 | upstream gene variant | G/A;C | snv | 2 |