Source: INFERRED ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28929495 | 0.807 | 0.120 | 7 | 55174014 | missense variant | G/A;C;T | snv | 3 | |||
rs7741164 | 0.882 | 0.080 | 6 | 41525674 | intron variant | G/A | snv | 6.6E-02 | 3 | ||
rs10429489 | 0.925 | 0.080 | 9 | 21787522 | intergenic variant | G/A | snv | 0.26 | 2 | ||
rs1200399 | 0.925 | 0.080 | 14 | 34823979 | intron variant | C/T | snv | 0.87 | 2 | ||
rs121913229 | 0.925 | 0.080 | 7 | 55174785 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
rs2293607 | 0.807 | 0.200 | 3 | 169764547 | non coding transcript exon variant | T/A;C | snv | 2 | |||
rs397516975 | 0.925 | 0.080 | 17 | 39724728 | inframe insertion | -/ATACGTGATGGC | delins | 2 | |||
rs4236709 | 0.925 | 0.080 | 8 | 32552592 | intron variant | G/A;T | snv | 2 | |||
rs55768116 | 0.925 | 0.080 | 11 | 118237616 | intron variant | C/A | snv | 0.38 | 2 |