Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1033656351 | 0.827 | 0.160 | 12 | 121232997 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 7 | |
rs6937506 | 0.807 | 0.280 | 6 | 132578260 | intergenic variant | G/A | snv | 0.25 | 7 | ||
rs1409851868 | 0.882 | 0.080 | 3 | 89399325 | missense variant | A/G | snv | 6 | |||
rs6903874 | 0.851 | 0.080 | 6 | 132575771 | downstream gene variant | T/C | snv | 0.23 | 5 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 5 | ||
rs1402757753 | 0.882 | 0.080 | 12 | 132621913 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs3916966 | 0.882 | 0.080 | 13 | 105458546 | upstream gene variant | C/A | snv | 0.63 | 4 | ||
rs7452939 | 0.882 | 0.080 | 6 | 132572626 | downstream gene variant | G/A | snv | 4 | |||
rs755302767 | 0.882 | 0.080 | 12 | 132621835 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs1935062 | 0.882 | 0.080 | 13 | 105475787 | intron variant | A/C | snv | 0.32 | 3 |