Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 32 | |||
rs61764370 | 0.662 | 0.320 | 12 | 25207290 | 3 prime UTR variant | A/C | snv | 6.2E-02 | 29 | ||
rs17851045 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 27 | ||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 24 | |||
rs712 | 0.677 | 0.360 | 12 | 25209618 | 3 prime UTR variant | A/C | snv | 0.46 | 24 | ||
rs121913238 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 17 | |||
rs727503109 | 0.752 | 0.320 | 12 | 25245277 | missense variant | T/C | snv | 17 | |||
rs104894360 | 0.724 | 0.560 | 12 | 25209904 | missense variant | T/A;C | snv | 14 | |||
rs121913535 | 0.742 | 0.320 | 12 | 25245348 | missense variant | C/A;G;T | snv | 14 | |||
rs121913528 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 12 | |||
rs104894365 | 0.827 | 0.320 | 12 | 25245345 | missense variant | C/T | snv | 9 | |||
rs104894366 | 0.776 | 0.400 | 12 | 25245284 | missense variant | G/A;C | snv | 9 | |||
rs121913527 | 0.807 | 0.320 | 12 | 25225628 | missense variant | C/A;G;T | snv | 9 | |||
rs770248150 | 0.807 | 0.240 | 12 | 25225713 | missense variant | T/A;G | snv | 4.0E-06 | 7 | ||
rs1057519725 | 0.851 | 0.320 | 12 | 25225627 | missense variant | G/A | snv | 7.0E-06 | 6 | ||
rs104894359 | 0.851 | 0.200 | 12 | 25227346 | missense variant | C/G;T | snv | 5 | |||
rs1137282 | 0.851 | 0.120 | 12 | 25209843 | missense variant | A/G;T | snv | 0.19 | 5 | ||
rs12587 | 0.827 | 0.200 | 12 | 25205894 | 3 prime UTR variant | T/G | snv | 0.49 | 5 | ||
rs7312175 | 0.827 | 0.120 | 12 | 25251670 | upstream gene variant | G/A | snv | 0.16 | 5 | ||
rs121913236 | 0.882 | 0.160 | 12 | 25245321 | missense variant | G/C;T | snv | 4 | |||
rs730880471 | 0.851 | 0.280 | 12 | 25225709 | missense variant | C/T | snv | 4 | |||
rs104894361 | 0.882 | 0.240 | 12 | 25245370 | missense variant | T/A;C;G | snv | 4.0E-06 | 3 | ||
rs104894362 | 0.882 | 0.200 | 12 | 25209894 | missense variant | G/C | snv | 3 |