Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs79184941 | 0.617 | 0.600 | 10 | 121520163 | missense variant | G/A;C | snv | 5.6E-05; 4.0E-06 | 41 | ||
rs77543610 | 0.667 | 0.560 | 10 | 121520160 | missense variant | G/C | snv | 28 | |||
rs121918487 | 0.716 | 0.440 | 10 | 121517378 | missense variant | C/A;G;T | snv | 25 | |||
rs121918491 | 0.716 | 0.440 | 10 | 121517371 | synonymous variant | C/T | snv | 4.0E-06 | 15 | ||
rs121909627 | 0.776 | 0.200 | 8 | 38424690 | missense variant | G/C | snv | 4.0E-06 | 8 | ||
rs121918488 | 0.790 | 0.120 | 10 | 121517379 | missense variant | A/C;G;T | snv | 7 | |||
rs776587763 | 0.790 | 0.120 | 10 | 121520085 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
rs121918501 | 0.807 | 0.080 | 10 | 121520050 | missense variant | A/C;G | snv | 6 | |||
rs777169135 | 0.851 | 0.080 | 10 | 121488064 | missense variant | T/C;G | snv | 4.0E-06 | 4 |