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 | ||
rs10189629 | 1.000 | 0.080 | 2 | 102263004 | regulatory region variant | C/A | snv | 0.15 | 2 | ||
rs10197862 | 0.925 | 0.120 | 2 | 102350089 | intron variant | A/G | snv | 0.18 | 2 | ||
rs1043828 | 1.000 | 0.080 | 5 | 111128310 | 3 prime UTR variant | T/C;G | snv | 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 | ||
rs11674302 | 1.000 | 0.080 | 2 | 102270668 | intergenic variant | T/C | snv | 0.16 | 2 | ||
rs11692065 | 1.000 | 0.080 | 2 | 102267515 | intergenic variant | C/T | snv | 0.15 | 2 | ||
rs11870965 | 0.925 | 0.160 | 17 | 39873952 | intron variant | T/A | snv | 0.40 | 3 | ||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 3 | ||
rs12603332 | 0.807 | 0.200 | 17 | 39926554 | 5 prime UTR variant | T/C | snv | 0.49 | 3 | ||
rs12936231 | 0.925 | 0.160 | 17 | 39872867 | intron variant | C/G;T | snv | 3 | |||
rs12950743 | 0.925 | 0.160 | 17 | 39892980 | intergenic variant | T/C | snv | 0.45 | 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 | ||
rs1342326 | 0.790 | 0.360 | 9 | 6190076 | intergenic variant | A/C | snv | 0.21 | 2 | ||
rs13431828 | 0.925 | 0.160 | 2 | 102338193 | 5 prime UTR variant | C/T | 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 | |||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 2 | ||
rs1888909 | 0.882 | 0.200 | 9 | 6197392 | downstream gene variant | T/A;C | snv | 2 | |||
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 |