Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1008723 | 0.925 | 0.160 | 17 | 39910014 | intron variant | G/C;T | snv | 3 | |||
rs10173081 | 1.000 | 0.080 | 2 | 102340888 | intron variant | C/T | snv | 0.18 | 2 | ||
rs10197862 | 0.925 | 0.120 | 2 | 102350089 | intron variant | A/G | snv | 0.18 | 2 | ||
rs10445308 | 0.851 | 0.240 | 17 | 39781794 | intron variant | C/T | snv | 0.38 | 3 | ||
rs11078925 | 0.925 | 0.160 | 17 | 39868955 | intron variant | T/C | snv | 0.36 | 3 | ||
rs11078927 | 0.925 | 0.080 | 17 | 39908152 | intron variant | C/T | snv | 0.40 | 0.35 | 2 | |
rs11870965 | 0.925 | 0.160 | 17 | 39873952 | intron variant | T/A | snv | 0.40 | 3 | ||
rs12936231 | 0.925 | 0.160 | 17 | 39872867 | intron variant | C/G;T | snv | 3 | |||
rs13408569 | 1.000 | 0.080 | 2 | 102338596 | intron variant | G/C | snv | 0.18 | 2 | ||
rs13408661 | 1.000 | 0.080 | 2 | 102338622 | intron variant | G/A | snv | 0.18 | 2 | ||
rs1362348 | 1.000 | 0.080 | 2 | 102368164 | intron variant | C/G | snv | 0.45 | 2 | ||
rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 7 | |||
rs17498196 | 1.000 | 0.080 | 9 | 6237547 | intron variant | A/C;G | snv | 2 | |||
rs204993 | 0.851 | 0.240 | 6 | 32187804 | intron variant | A/G | snv | 0.24 | 0.26 | 3 | |
rs2066362 | 1.000 | 0.080 | 9 | 6219176 | intron variant | G/C;T | snv | 2 | |||
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 6 | ||
rs3755276 | 0.925 | 0.120 | 2 | 102361999 | intron variant | C/T | snv | 0.45 | 2 | ||
rs3771166 | 1.000 | 0.080 | 2 | 102369762 | intron variant | G/A;T | snv | 2 | |||
rs3816470 | 0.925 | 0.160 | 17 | 39829548 | intron variant | A/G | snv | 0.54 | 3 | ||
rs4794820 | 0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv | 3 | |||
rs4795400 | 0.925 | 0.080 | 17 | 39910767 | intron variant | C/T | snv | 0.36 | 3 | ||
rs4795405 | 0.851 | 0.160 | 17 | 39932164 | intron variant | T/A;C | snv | 3 | |||
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 3 | ||
rs8076131 | 0.790 | 0.200 | 17 | 39924659 | intron variant | G/A;C | snv | 3 | |||
rs869402 | 0.925 | 0.160 | 17 | 39911790 | intron variant | T/A;C | snv | 3 |