Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137852564 | 0.827 | 0.240 | X | 67722976 | missense variant | G/A;T | snv | 3 | |||
rs55770810 | 0.763 | 0.280 | 17 | 43063931 | missense variant | G/A;T | snv | 2.4E-05; 8.0E-06 | 3 | ||
rs80357474 | 0.827 | 0.200 | 17 | 43049188 | missense variant | A/C;G;T | snv | 8.0E-06 | 3 | ||
rs121964872 | 0.882 | 0.120 | 16 | 68833362 | missense variant | A/G | snv | 4.4E-05 | 1.1E-04 | 3 | |
rs121913413 | 0.763 | 0.240 | 3 | 41224634 | missense variant | C/A;T | snv | 3 | |||
rs121913403 | 0.683 | 0.240 | 3 | 41224622 | missense variant | C/A;G;T | snv | 3 | |||
rs61753793 | 0.851 | 0.120 | 2 | 47799002 | missense variant | T/C | snv | 3.6E-05 | 5.6E-05 | 3 | |
rs776587763 | 0.790 | 0.120 | 10 | 121520085 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs121918502 | 0.790 | 0.160 | 10 | 121517351 | missense variant | G/C | snv | 3 | |||
rs28936683 | 0.882 | 0.080 | 20 | 35434093 | missense variant | A/G | snv | 7.0E-06 | 3 | ||
rs121909352 | 0.882 | 0.120 | 8 | 96145185 | missense variant | G/T | snv | 2.0E-03 | 2.0E-03 | 3 | |
rs36119840 | 0.807 | 0.280 | 5 | 37816010 | missense variant | G/A | snv | 2.3E-03 | 2.7E-03 | 3 | |
rs192732174 | 0.827 | 0.160 | 3 | 33068245 | missense variant | G/A;T | snv | 4.0E-05; 3.6E-05 | 3 | ||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
rs57520892 | 0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 | 3 | ||
rs60890628 | 0.776 | 0.200 | 1 | 156138507 | missense variant | C/T | snv | 1.5E-04 | 1.0E-04 | 3 | |
rs121908670 | 0.882 | 0.080 | 11 | 68363784 | missense variant | G/A | snv | 3 | |||
rs28940291 | 0.776 | 0.080 | 1 | 11992660 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
rs281865127 | 0.827 | 0.120 | 1 | 161306767 | missense variant | T/C | snv | 3 | |||
rs63750664 | 0.882 | 0.200 | 2 | 47783292 | missense variant | C/A;T | snv | 4.1E-06; 9.4E-05 | 3 | ||
rs2020912 | 0.807 | 0.480 | 2 | 47800616 | missense variant | T/C;G | snv | 5.1E-03 | 3 | ||
rs104894119 | 0.807 | 0.160 | 9 | 124500685 | missense variant | C/T | snv | 3 | |||
rs121913272 | 0.752 | 0.400 | 3 | 179210192 | missense variant | T/C;G | snv | 3 | |||
rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 3 |