Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 16 | |||
rs11210892 | 1.000 | 0.040 | 1 | 43634413 | intergenic variant | G/A | snv | 0.51 | 3 | ||
rs4664442 | 1.000 | 0.040 | 2 | 161971491 | intron variant | G/A;C | snv | 3 | |||
rs11783093 | 1.000 | 0.040 | 8 | 27567832 | intron variant | C/T | snv | 0.11 | 2 |