Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1386483 | 0.790 | 0.080 | 12 | 72018714 | intron variant | T/C | snv | 0.53 | 9 | ||
rs9834970 | 0.790 | 0.080 | 3 | 36814539 | downstream gene variant | T/C | snv | 0.45 | 9 | ||
rs1469698992 | 0.776 | 0.080 | 9 | 131190453 | missense variant | G/A | snv | 8 | |||
rs147837176 | 0.776 | 0.080 | 5 | 1400949 | missense variant | T/C | snv | 3.1E-04 | 2.8E-04 | 8 | |
rs1062613 | 0.807 | 0.080 | 11 | 113975284 | 5 prime UTR variant | T/C | snv | 0.79 | 0.71 | 7 | |
rs17110563 | 0.827 | 0.080 | 12 | 71972526 | missense variant | C/T | snv | 1.2E-03 | 1.1E-03 | 7 | |
rs766288 | 0.790 | 0.080 | 1 | 231557942 | intron variant | G/T | snv | 0.40 | 7 | ||
rs2076137 | 0.807 | 0.080 | 22 | 50077337 | intron variant | C/T | snv | 0.14 | 6 | ||
rs2235349 | 0.807 | 0.080 | 22 | 50079810 | intron variant | T/C | snv | 0.22 | 6 | ||
rs2812393 | 0.807 | 0.080 | 1 | 231777927 | intron variant | G/C | snv | 0.61 | 6 | ||
rs707284 | 0.807 | 0.080 | 2 | 211974321 | intron variant | T/A;C | snv | 6 | |||
rs1106854 | 0.827 | 0.080 | 2 | 75050887 | intron variant | T/C;G | snv | 5 | |||
rs1386482 | 0.827 | 0.080 | 12 | 72018792 | intron variant | T/G | snv | 0.52 | 5 | ||
rs1386486 | 0.827 | 0.080 | 12 | 72018440 | intron variant | A/G | snv | 0.53 | 5 | ||
rs166508 | 0.827 | 0.080 | 3 | 37548944 | intron variant | T/C | snv | 0.44 | 5 | ||
rs2839350 | 0.827 | 0.080 | 21 | 46597307 | downstream gene variant | G/A | snv | 0.22 | 5 | ||
rs34608001 | 0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 | 5 | |
rs3831455 | 0.827 | 0.080 | 11 | 113904828 | 5 prime UTR variant | GAG/- | delins | 5 | |||
rs839523 | 0.827 | 0.080 | 2 | 211951364 | intron variant | C/T | snv | 0.40 | 5 | ||
rs2251219 | 0.732 | 0.120 | 3 | 52550771 | synonymous variant | T/C;G | snv | 0.39; 4.0E-06 | 0.34 | 14 | |
rs3771829 | 0.790 | 0.120 | 2 | 75137019 | intron variant | C/G | snv | 0.11 | 9 | ||
rs3788266 | 0.732 | 0.160 | 21 | 46606442 | upstream gene variant | G/A | snv | 0.50 | 12 | ||
rs821616 | 0.752 | 0.200 | 1 | 232008852 | missense variant | A/T | snv | 0.26 | 0.29 | 13 | |
rs1176744 | 0.708 | 0.240 | 11 | 113932306 | missense variant | A/C | snv | 0.33 | 0.36 | 19 | |
rs4988483 | 0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 | 11 |