Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 6 | |||||
rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
rs2287922 | 19 | 48728969 | missense variant | G/A | snv | 0.37 | 0.37 | 3 |