Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10223646 | 0.882 | 0.080 | 6 | 116296236 | intron variant | C/T | snv | 0.41 | 4 | ||
rs760761 | 0.882 | 0.080 | 6 | 15650901 | intron variant | G/A | snv | 0.26 | 4 | ||
rs1106634 | 0.851 | 0.080 | 8 | 20208538 | intron variant | G/A;C;T | snv | 0.18 | 5 | ||
rs11904814 | 0.851 | 0.080 | 2 | 207562074 | intron variant | T/G | snv | 0.30 | 5 | ||
rs12912233 | 0.851 | 0.120 | 15 | 60974897 | intron variant | C/T | snv | 0.38 | 5 | ||
rs174697 | 0.851 | 0.080 | 22 | 19966309 | intron variant | A/G | snv | 0.88 | 5 | ||
rs4648308 | 0.851 | 0.160 | 1 | 186671485 | downstream gene variant | C/T | snv | 0.27 | 5 | ||
rs528732638 | 0.851 | 0.120 | 18 | 26940224 | intron variant | A/-;AA;AAA;AAAA | delins | 5 | |||
rs61888800 | 0.851 | 0.080 | 11 | 27700731 | 5 prime UTR variant | G/T | snv | 0.19 | 5 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 5 | ||
rs766020740 | 0.851 | 0.120 | 22 | 19963644 | missense variant | C/A | snv | 4.0E-06 | 5 | ||
rs794727961 | 0.851 | 0.080 | 12 | 2512979 | missense variant | G/A | snv | 5 | |||
rs9825823 | 0.851 | 0.080 | 3 | 61096480 | intron variant | T/C | snv | 0.47 | 5 | ||
rs10514299 | 0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 | 6 | ||
rs1545843 | 0.827 | 0.120 | 12 | 84170289 | intron variant | G/A | snv | 0.52 | 6 | ||
rs2253206 | 0.851 | 0.080 | 2 | 207527254 | intron variant | A/G | snv | 0.47 | 6 | ||
rs2619522 | 0.827 | 0.080 | 6 | 15653418 | intron variant | A/C | snv | 0.26 | 6 | ||
rs28386840 | 0.827 | 0.080 | 16 | 55652906 | upstream gene variant | T/A;C | snv | 6 | |||
rs120074175 | 0.827 | 0.080 | 12 | 72031544 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 7 | |
rs1415125856 | 0.827 | 0.120 | 11 | 27658550 | splice region variant | G/A | snv | 4.0E-06 | 2.1E-05 | 7 | |
rs1818879 | 0.827 | 0.120 | 7 | 22733108 | downstream gene variant | G/A;C | snv | 7 | |||
rs2522833 | 0.827 | 0.080 | 7 | 82824392 | missense variant | A/C | snv | 0.45 | 0.34 | 7 | |
rs6937506 | 0.807 | 0.280 | 6 | 132578260 | intergenic variant | G/A | snv | 0.25 | 7 | ||
rs776943620 | 0.851 | 0.120 | 17 | 63477287 | missense variant | G/A | snv | 2.1E-05 | 7 | ||
rs7305115 | 0.807 | 0.200 | 12 | 71979082 | synonymous variant | A/C;G;T | snv | 4.0E-06; 0.56 | 8 |