Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913603 | 0.732 | 0.160 | 1 | 161306722 | missense variant | T/C;G | snv | 2.0E-05 | 12 | ||
rs121913595 | 0.742 | 0.160 | 1 | 161306785 | missense variant | G/A;T | snv | 11 | |||
rs28928910 | 0.827 | 0.200 | 8 | 24956452 | missense variant | G/A;T | snv | 11 | |||
rs121913586 | 0.752 | 0.200 | 1 | 161306414 | missense variant | C/G;T | snv | 10 | |||
rs58982919 | 0.790 | 0.080 | 8 | 24956223 | missense variant | T/C | snv | 10 | |||
rs104894619 | 0.827 | 0.120 | 17 | 15231047 | missense variant | G/A | snv | 4.0E-03 | 3.7E-03 | 9 | |
rs104894621 | 0.790 | 0.080 | 17 | 15239575 | missense variant | G/A | snv | 9 | |||
rs1553259648 | 0.776 | 0.160 | 1 | 161306759 | missense variant | G/C;T | snv | 8 | |||
rs121913589 | 0.827 | 0.200 | 1 | 161306863 | missense variant | C/A;G;T | snv | 7 | |||
rs1553259662 | 0.827 | 0.200 | 1 | 161306821 | missense variant | A/G | snv | 7 | |||
rs104894161 | 0.807 | 0.080 | 10 | 62813563 | missense variant | G/A | snv | 6 | |||
rs104894159 | 0.827 | 0.080 | 10 | 62813413 | missense variant | G/A | snv | 5 | |||
rs121913590 | 0.851 | 0.080 | 1 | 161306864 | missense variant | G/A | snv | 7.0E-06 | 5 | ||
rs121913598 | 0.851 | 0.080 | 1 | 161307361 | missense variant | G/A | snv | 5 | |||
rs281865127 | 0.827 | 0.120 | 1 | 161306767 | missense variant | T/C | snv | 5 | |||
rs281865128 | 0.882 | 0.080 | 1 | 161306426 | missense variant | C/G;T | snv | 5 | |||
rs371856018 | 0.882 | 0.120 | 1 | 161307376 | missense variant | T/C;G | snv | 8.0E-06 | 5 | ||
rs281865137 | 0.851 | 0.080 | 10 | 62813496 | missense variant | C/T | snv | 4 | |||
rs121913585 | 0.851 | 0.080 | 1 | 161307304 | missense variant | G/A;C | snv | 4 | |||
rs121913596 | 0.851 | 0.080 | 1 | 161307389 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs121913601 | 0.851 | 0.080 | 1 | 161307259 | missense variant | G/A;C | snv | 4 | |||
rs1553259707 | 0.851 | 0.080 | 1 | 161306911 | missense variant | T/C | snv | 4 | |||
rs572010627 | 0.851 | 0.160 | 1 | 161306738 | missense variant | A/C;T | snv | 8.0E-06 | 4 | ||
rs104894617 | 0.851 | 0.080 | 17 | 15260681 | missense variant | A/G | snv | 4 | |||
rs104894623 | 0.851 | 0.200 | 17 | 15239591 | missense variant | C/G;T | snv | 4 |