Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
rs121909231 | 0.667 | 0.600 | 10 | 87961095 | stop gained | C/A;T | snv | 32 | |||
rs121909218 | 0.672 | 0.360 | 10 | 87933145 | missense variant | G/A | snv | 25 | |||
rs121909219 | 0.689 | 0.400 | 10 | 87957915 | stop gained | C/A;T | snv | 25 | |||
rs712 | 0.677 | 0.360 | 12 | 25209618 | 3 prime UTR variant | A/C | snv | 0.46 | 24 | ||
rs786204858 | 0.776 | 0.280 | 10 | 87933079 | missense variant | A/G;T | snv | 11 | |||
rs1432155504 | 1.000 | 0.080 | 22 | 21225543 | missense variant | C/G | snv | 1 | |||
rs4745021 | 1.000 | 0.080 | 9 | 70652691 | intron variant | T/A;G | snv | 1 | |||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 34 | ||
rs1179469165 | 0.925 | 0.080 | 14 | 81143917 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs121909224 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 41 | ||
rs1800472 | 0.752 | 0.360 | 19 | 41341955 | missense variant | G/A | snv | 2.6E-02 | 2.3E-02 | 11 | |
rs1800862 | 0.925 | 0.160 | 10 | 43119646 | synonymous variant | C/T | snv | 4.5E-02 | 3.9E-02 | 2 | |
rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 |