Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs796052243 | 0.695 | 0.520 | 4 | 122934574 | inframe deletion | CAA/- | delins | 54 | |||
rs121909231 | 0.667 | 0.600 | 10 | 87961095 | stop gained | C/A;T | snv | 32 | |||
rs16862780 | 0.925 | 0.080 | 3 | 187970052 | intron variant | G/A;T | snv | 3 | |||
rs10905875 | 0.925 | 0.080 | 10 | 6131814 | intergenic variant | G/A;C | snv | 2 | |||
rs116041786 | 0.925 | 0.080 | 6 | 32634619 | intron variant | C/T | snv | 2 | |||
rs1244181 | 0.925 | 0.080 | 10 | 8049414 | intron variant | A/C;G | snv | 2 | |||
rs2136613 | 0.925 | 0.080 | 10 | 62834404 | intron variant | C/G;T | snv | 2 | |||
rs34069391 | 0.925 | 0.080 | 16 | 11067358 | intron variant | T/- | delins | 2 | |||
rs67257959 | 0.925 | 0.080 | 19 | 17047335 | upstream gene variant | T/A;C | snv | 2 | |||
rs812936 | 1.000 | 0.080 | 19 | 5844638 | missense variant | G/A;C | snv | 0.83 | 2 | ||
rs80168506 | 0.925 | 0.080 | 2 | 213196729 | intergenic variant | A/G | snv | 5.1E-02 | 2 | ||
rs12967678 | 0.925 | 0.080 | 18 | 12805389 | intron variant | G/A | snv | 8.0E-02 | 2 | ||
rs146583707 | 0.925 | 0.080 | 4 | 122571262 | intergenic variant | T/A | snv | 0.20 | 2 | ||
rs12257092 | 0.925 | 0.080 | 10 | 89023070 | intergenic variant | A/T | snv | 0.27 | 2 | ||
rs11299600 | 0.925 | 0.080 | 8 | 128192327 | regulatory region variant | A/- | delins | 0.29 | 2 | ||
rs10071761 | 0.925 | 0.080 | 5 | 40415509 | intron variant | T/C | snv | 0.31 | 2 | ||
rs9831894 | 0.882 | 0.120 | 3 | 122081640 | intron variant | A/C | snv | 0.31 | 3 | ||
rs4565870 | 0.925 | 0.080 | 11 | 46328319 | upstream gene variant | T/C | snv | 0.43 | 2 | ||
rs601338 | 0.742 | 0.280 | 19 | 48703417 | stop gained | G/A | snv | 0.38 | 0.45 | 19 | |
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 33 | |
rs8071789 | 0.925 | 0.080 | 17 | 39850080 | intron variant | C/T | snv | 0.47 | 2 | ||
rs2210913 | 0.925 | 0.080 | 1 | 157699203 | intron variant | C/T | snv | 0.56 | 2 | ||
rs7773987 | 0.925 | 0.080 | 6 | 135386348 | intron variant | C/T | snv | 0.60 | 2 | ||
rs778986 | 1.000 | 0.080 | 19 | 5844526 | missense variant | A/G | snv | 0.84 | 0.84 | 3 | |
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 |