Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 25 | ||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 16 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 16 | ||
rs17817449 | 0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv | 7 | |||
rs10196867 | 0.925 | 0.080 | 2 | 79751234 | intron variant | C/G;T | snv | 5 | |||
rs11066001 | 0.763 | 0.360 | 12 | 111681367 | intron variant | T/C | snv | 5.8E-03 | 5 | ||
rs147247472 | 0.925 | 0.080 | 1 | 49441901 | intron variant | G/A | snv | 7.3E-04 | 5 | ||
rs2133896 | 0.925 | 0.080 | 12 | 99455122 | intron variant | G/T | snv | 7.6E-02 | 5 | ||
rs11681792 | 1.000 | 0.080 | 2 | 49957256 | intron variant | C/T | snv | 0.12 | 4 | ||
rs11825659 | 0.925 | 0.080 | 11 | 133925624 | intron variant | A/G | snv | 0.12 | 4 | ||
rs12544026 | 0.925 | 0.080 | 8 | 101819970 | intron variant | G/A | snv | 0.85 | 4 | ||
rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 | ||
rs17028615 | 1.000 | 0.080 | 4 | 99150767 | intron variant | A/C;G | snv | 4 | |||
rs2094081 | 0.925 | 0.080 | 1 | 38927359 | intron variant | G/A;C | snv | 4 | |||
rs58598658 | 0.925 | 0.080 | 13 | 73887725 | intron variant | -/A;AA | delins | 4 | |||
rs72737330 | 0.925 | 0.080 | 1 | 216600151 | intron variant | T/C | snv | 0.15 | 4 | ||
rs79246196 | 0.925 | 0.080 | 7 | 100185286 | intron variant | C/T | snv | 1.8E-02 | 4 | ||
rs1000579 | 1.000 | 0.080 | 4 | 4717767 | intron variant | A/G | snv | 0.44 | 3 | ||
rs10211296 | 1.000 | 0.080 | 2 | 165633833 | intron variant | A/G | snv | 0.34 | 3 | ||
rs10483038 | 1.000 | 0.080 | 21 | 37652469 | intron variant | T/C | snv | 0.26 | 3 | ||
rs11075992 | 1.000 | 0.080 | 16 | 53786154 | intron variant | T/C | snv | 0.41 | 3 | ||
rs111372083 | 1.000 | 0.080 | 21 | 37638374 | intron variant | C/A;T | snv | 0.27 | 3 | ||
rs1154433 | 1.000 | 0.080 | 4 | 99332551 | intron variant | A/G;T | snv | 3 | |||
rs115460205 | 1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
rs12482570 | 1.000 | 0.080 | 21 | 37705475 | intron variant | A/G | snv | 0.30 | 3 |