Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 18 | ||
rs10237735 | 7 | 32337136 | intron variant | C/T | snv | 7.6E-02 | 2 | ||||
rs10414689 | 19 | 51293045 | regulatory region variant | T/C | snv | 0.11 | 2 | ||||
rs10809457 | 9 | 11402319 | intron variant | G/T | snv | 0.36 | 2 | ||||
rs11119805 | 1 | 211744902 | 3 prime UTR variant | T/A | snv | 0.13 | 2 | ||||
rs11120822 | 1 | 7053052 | intron variant | G/C | snv | 0.34 | 2 | ||||
rs11190604 | 10 | 100542700 | intron variant | A/G | snv | 0.19 | 2 | ||||
rs12098564 | 10 | 85193571 | non coding transcript exon variant | A/G | snv | 7.4E-02 | 2 | ||||
rs12529874 | 6 | 98014625 | intron variant | G/A | snv | 2.6E-02 | 2 | ||||
rs174541 | 1.000 | 0.080 | 11 | 61798436 | intron variant | T/C | snv | 0.29 | 8 | ||
rs174550 | 0.925 | 0.160 | 11 | 61804006 | 5 prime UTR variant | T/C | snv | 0.28 | 13 | ||
rs174556 | 0.925 | 0.160 | 11 | 61813163 | intron variant | C/T | snv | 0.26 | 7 | ||
rs17648246 | 13 | 44919746 | intergenic variant | A/G | snv | 5.0E-02 | 2 | ||||
rs2118674 | 2 | 170462384 | intron variant | A/T | snv | 0.87 | 2 | ||||
rs2366017 | 17 | 69854760 | intron variant | G/A | snv | 2.1E-02 | 2 | ||||
rs2391388 | 1 | 95020269 | intron variant | A/C | snv | 0.49 | 2 | ||||
rs3134950 | 6 | 32159700 | intron variant | C/A | snv | 0.64 | 2 | ||||
rs334809 | 0.925 | 0.080 | 3 | 3088537 | intron variant | A/G;T | snv | 4 | |||
rs4246215 | 0.677 | 0.320 | 11 | 61796827 | 3 prime UTR variant | G/C;T | snv | 29 | |||
rs4465599 | 16 | 13061021 | intron variant | G/A | snv | 0.69 | 2 | ||||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs6671200 | 1 | 95231973 | intron variant | A/C | snv | 0.90 | 2 | ||||
rs6675668 | 1 | 95050081 | intron variant | T/G | snv | 0.43 | 2 | ||||
rs6722456 | 2 | 133771520 | intergenic variant | G/A | snv | 4.5E-02 | 2 | ||||
rs742614 | 20 | 33894826 | intergenic variant | A/G;T | snv | 2 |