Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11792633 | 0.882 | 0.280 | 9 | 6248035 | intron variant | C/T | snv | 0.35 | 5 | ||
rs678849 | 0.882 | 0.120 | 1 | 28818676 | intron variant | C/T | snv | 0.44 | 5 | ||
rs1800498 | 0.882 | 0.080 | 11 | 113420866 | intron variant | G/A | snv | 0.44 | 4 | ||
rs279826 | 1.000 | 0.080 | 4 | 46332192 | intron variant | A/G | snv | 0.46 | 4 | ||
rs4537731 | 1.000 | 0.040 | 11 | 18047335 | upstream gene variant | T/C | snv | 0.48 | 3 | ||
rs4675690 | 2 | 207643083 | intergenic variant | C/T | snv | 0.48 | 3 | ||||
rs12701020 | 0.925 | 0.040 | 7 | 30655345 | intron variant | C/T | snv | 0.12 | 3 | ||
rs10947563 | 0.925 | 0.040 | 6 | 35685660 | intron variant | G/A | snv | 0.77 | 3 | ||
rs3798347 | 0.925 | 0.040 | 6 | 35633999 | intron variant | A/T | snv | 0.65 | 3 | ||
rs56372821 | 1.000 | 0.080 | 8 | 27578983 | intron variant | G/A | snv | 0.13 | 2 | ||
rs9316235 | 13 | 46871568 | intron variant | G/A | snv | 0.19 | 2 | ||||
rs1885884 | 13 | 46856141 | non coding transcript exon variant | C/A;G;T | snv | 2 | |||||
rs9829896 | 3 | 20135980 | intron variant | C/A;T | snv | 2 | |||||
rs893290 | 15 | 61190958 | intron variant | G/T | snv | 0.96 | 1 |