Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913595 | 0.742 | 0.160 | 1 | 161306785 | missense variant | G/A;T | snv | 4 | |||
rs281865127 | 0.827 | 0.120 | 1 | 161306767 | missense variant | T/C | snv | 3 | |||
rs104894161 | 0.807 | 0.080 | 10 | 62813563 | missense variant | G/A | snv | 2 | |||
rs104894826 | 0.882 | 0.080 | X | 71224114 | missense variant | T/C | snv | 2 | |||
rs121913585 | 0.851 | 0.080 | 1 | 161307304 | missense variant | G/A;C | snv | 2 | |||
rs121913586 | 0.752 | 0.200 | 1 | 161306414 | missense variant | C/G;T | snv | 2 | |||
rs121913590 | 0.851 | 0.080 | 1 | 161306864 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs121913597 | 0.827 | 0.160 | 1 | 161307268 | missense variant | T/A | snv | 2 | |||
rs1553259707 | 0.851 | 0.080 | 1 | 161306911 | missense variant | T/C | snv | 2 | |||
rs879253858 | 0.882 | 0.120 | 1 | 161306753 | missense variant | T/G | snv | 2 | |||
rs104894617 | 0.851 | 0.080 | 17 | 15260681 | missense variant | A/G | snv | 2 | |||
rs104894621 | 0.790 | 0.080 | 17 | 15239575 | missense variant | G/A | snv | 2 | |||
rs104894159 | 0.827 | 0.080 | 10 | 62813413 | missense variant | G/A | snv | 1 | |||
rs121913601 | 0.851 | 0.080 | 1 | 161307259 | missense variant | G/A;C | snv | 1 | |||
rs121913603 | 0.732 | 0.160 | 1 | 161306722 | missense variant | T/C;G | snv | 2.0E-05 | 1 | ||
rs267607241 | 1.000 | 0.080 | 1 | 161306815 | missense variant | A/G | snv | 1 | |||
rs267607242 | 1.000 | 0.080 | 1 | 161306810 | missense variant | T/G | snv | 1 | |||
rs267607243 | 0.925 | 0.080 | 1 | 161306774 | missense variant | C/T | snv | 1 | |||
rs770546306 | 0.882 | 0.080 | 1 | 161307402 | missense variant | G/A;C;T | snv | 3.2E-05; 5.2E-05 | 1 | ||
rs104894620 | 0.925 | 0.080 | 17 | 15239584 | start lost | A/G;T | snv | 1 | |||
rs104894622 | 0.882 | 0.080 | 17 | 15260692 | missense variant | G/T | snv | 1 | |||
rs104894624 | 0.925 | 0.080 | 17 | 15230952 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
rs28936682 | 1.000 | 0.080 | 17 | 15230931 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs775019409 | 1.000 | 0.080 | 17 | 15230953 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||
rs879253954 | 0.882 | 0.160 | 17 | 15230951 | missense variant | C/A;T | snv | 1 |