Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2236479 | 0.925 | 0.160 | 21 | 45499218 | intron variant | G/A | snv | 0.40 | 2 | ||
rs2255280 | 0.925 | 0.120 | 5 | 39394887 | intron variant | C/A | snv | 0.98 | 2 | ||
rs2457571 | 0.925 | 0.120 | 6 | 160413796 | intron variant | T/C | snv | 0.62 | 2 | ||
rs2470353 | 0.925 | 0.120 | 3 | 14148768 | intron variant | G/A;C;T | snv | 0.41; 1.5E-04 | 2 | ||
rs2980874 | 0.925 | 0.120 | 8 | 125432546 | intron variant | G/A | snv | 0.30 | 2 | ||
rs3124761 | 0.925 | 0.120 | 9 | 133474633 | intron variant | T/C | snv | 0.80 | 2 | ||
rs34852782 | 0.925 | 0.120 | 7 | 151869086 | intron variant | -/A;AG | ins | 2 | |||
rs3729587 | 0.925 | 0.120 | 3 | 14167125 | intron variant | G/C | snv | 0.31 | 0.34 | 2 | |
rs3731055 | 0.925 | 0.120 | 3 | 14178939 | intron variant | C/T | snv | 1.9E-02 | 2 | ||
rs3731114 | 0.925 | 0.120 | 3 | 14165122 | intron variant | C/G | snv | 1.8E-02 | 2 | ||
rs4795218 | 0.925 | 0.120 | 17 | 37718512 | intron variant | A/G | snv | 0.82 | 2 | ||
rs4927850 | 0.925 | 0.120 | 3 | 196024759 | intron variant | T/C | snv | 0.71 | 2 | ||
rs5757573 | 0.925 | 0.120 | 22 | 39237617 | intron variant | C/T | snv | 0.57 | 2 | ||
rs5768709 | 0.925 | 0.120 | 22 | 48533757 | intron variant | A/G | snv | 0.36 | 2 | ||
rs6001516 | 0.925 | 0.120 | 22 | 39248198 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs6127119 | 0.925 | 0.120 | 20 | 54162543 | intron variant | C/T | snv | 0.24 | 2 | ||
rs62068300 | 0.925 | 0.120 | 17 | 80600927 | intron variant | G/A;T | snv | 5.7E-05 | 2 | ||
rs6464375 | 0.925 | 0.120 | 7 | 153928758 | intron variant | C/T | snv | 6.7E-02 | 2 | ||
rs6475609 | 0.925 | 0.120 | 9 | 22106272 | intron variant | A/C;G;T | snv | 2 | |||
rs708224 | 0.925 | 0.120 | 12 | 32283475 | intron variant | A/G | snv | 0.50 | 2 | ||
rs78417682 | 0.925 | 0.120 | 7 | 47449305 | intron variant | G/C | snv | 0.15 | 2 | ||
rs1153287 | 1.000 | 0.120 | 21 | 29313290 | intron variant | G/A;T | snv | 1 | |||
rs1153294 | 1.000 | 0.120 | 21 | 29328775 | intron variant | T/C;G | snv | 1 | |||
rs117214 | 1.000 | 0.120 | 21 | 29348513 | intron variant | C/T | snv | 0.45 | 1 | ||
rs1975920 | 1.000 | 0.120 | 12 | 27583053 | intron variant | G/T | snv | 0.40 | 1 |