Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
rs79184941 | 0.617 | 0.600 | 10 | 121520163 | missense variant | G/A;C | snv | 5.6E-05; 4.0E-06 | 41 | ||
rs1564919048 | 0.732 | 0.280 | 10 | 121520106 | missense variant | C/A | snv | 23 | |||
rs1554122802 | 0.742 | 0.160 | 5 | 128335170 | missense variant | C/T | snv | 22 | |||
rs1318358361 | 0.724 | 0.240 | 6 | 156778678 | missense variant | C/G | snv | 2.1E-05 | 13 | ||
rs374608214 | 0.742 | 0.160 | 10 | 121520010 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 13 | |
rs1884302 | 0.851 | 0.120 | 20 | 7125642 | intron variant | T/C | snv | 0.41 | 4 | ||
rs10262453 | 0.925 | 0.080 | 7 | 33216427 | intron variant | A/C | snv | 0.27 | 2 |