Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10276782 | 1.000 | 0.040 | 7 | 24765621 | regulatory region variant | C/T | snv | 0.13 | 1 | ||
rs562020 | 1.000 | 0.040 | 13 | 33017932 | intron variant | A/G | snv | 0.69 | 1 | ||
rs567170 | 1.000 | 0.040 | 13 | 33043649 | intron variant | C/G | snv | 0.32 | 1 | ||
rs11781551 | 1.000 | 0.040 | 8 | 122395852 | intergenic variant | G/A | snv | 0.40 | 1 | ||
rs17045031 | 1.000 | 0.040 | 3 | 66717940 | intergenic variant | G/A | snv | 0.10 | 1 | ||
rs747885829 | 1.000 | 0.040 | 1 | 247423957 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 1 | |
rs6601530 | 1.000 | 0.040 | 8 | 10813762 | intron variant | G/A | snv | 0.61 | 1 | ||
rs4552883 | 0.925 | 0.040 | 8 | 139234730 | regulatory region variant | G/A;C | snv | 2 | |||
rs6918289 | 0.925 | 0.040 | 6 | 41134089 | intron variant | G/T | snv | 9.8E-02 | 2 | ||
rs138227502 | 0.925 | 0.040 | 3 | 186853221 | missense variant | C/T | snv | 1.8E-04 | 5.6E-04 | 2 | |
rs915014 | 0.925 | 0.040 | 1 | 11789412 | missense variant | T/C | snv | 2 | |||
rs4142986 | 0.925 | 0.040 | 9 | 99052344 | intron variant | C/A;G;T | snv | 1.1E-04; 0.75; 4.0E-06 | 2 | ||
rs495392 | 1.000 | 0.040 | 13 | 33018055 | intron variant | C/A | snv | 0.24 | 2 | ||
rs769442590 | 0.925 | 0.040 | 8 | 19960927 | missense variant | A/C;G | snv | 1.6E-05 | 2 | ||
rs767523236 | 0.925 | 0.040 | 17 | 58279033 | missense variant | T/C | snv | 4.1E-06 | 7.0E-06 | 2 | |
rs13447720 | 0.925 | 0.040 | 11 | 94432160 | intron variant | T/C | snv | 0.17 | 2 | ||
rs499952 | 0.925 | 0.040 | 11 | 94449826 | intron variant | G/T | snv | 0.41 | 2 | ||
rs749582333 | 0.925 | 0.040 | 11 | 89340157 | frameshift variant | G/- | delins | 2 | |||
rs7177922 | 0.925 | 0.040 | 15 | 33616418 | intron variant | G/A | snv | 0.19 | 2 | ||
rs4901536 | 0.925 | 0.080 | 14 | 54733816 | intron variant | T/C | snv | 0.67 | 2 | ||
rs750996166 | 0.925 | 0.040 | 1 | 161041409 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs17398575 | 0.882 | 0.040 | 7 | 106769006 | intron variant | G/A | snv | 0.20 | 3 | ||
rs7833904 | 0.882 | 0.040 | 8 | 58505103 | upstream gene variant | A/T | snv | 0.55 | 3 | ||
rs8042271 | 0.882 | 0.040 | 15 | 89030987 | intergenic variant | G/A;T | snv | 3 | |||
rs28937313 | 0.882 | 0.160 | 9 | 104822520 | missense variant | T/C | snv | 8.0E-06 | 3 |