Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11012732 | 0.882 | 0.080 | 10 | 21541175 | intron variant | A/G | snv | 0.31 | 5 | ||
rs121918347 | 0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv | 4 | |||
rs12770228 | 0.882 | 0.080 | 10 | 21494705 | non coding transcript exon variant | G/A | snv | 0.24 | 4 | ||
rs3219466 | 0.851 | 0.080 | 1 | 45340381 | 5 prime UTR variant | G/A;T | snv | 4 | |||
rs2686876 | 0.882 | 0.080 | 11 | 258909 | intergenic variant | T/A;C | snv | 3 | |||
rs7574920 | 0.882 | 0.080 | 2 | 31362783 | intron variant | G/C | snv | 0.42 | 3 | ||
rs768803947 | 0.882 | 0.080 | 17 | 7670624 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs202247756 | 1.000 | 0.080 | 10 | 102550019 | missense variant | C/T | snv | 2 | |||
rs1329443726 | 1.000 | 0.080 | 9 | 21971097 | frameshift variant | C/- | delins | 1 | |||
rs1475218156 | 1.000 | 0.080 | 9 | 22006096 | missense variant | C/G;T | snv | 4.2E-06; 8.4E-06 | 1 | ||
rs1568234664 | 1.000 | 0.080 | 19 | 10154774 | splice acceptor variant | C/A | snv | 1 | |||
rs587776563 | 1.000 | 0.080 | 22 | 29668440 | frameshift variant | A/- | delins | 1 | |||
rs1035938 | 0.776 | 0.120 | 19 | 47680514 | missense variant | C/G;T | snv | 0.29 | 8 | ||
rs25406 | 0.807 | 0.120 | 20 | 5118990 | intron variant | G/A | snv | 0.41 | 8 | ||
rs4968451 | 0.732 | 0.160 | 17 | 61849946 | intron variant | A/C | snv | 0.15 | 13 | ||
rs1243180 | 0.790 | 0.160 | 10 | 21626690 | intron variant | T/A | snv | 0.23 | 7 | ||
rs267606541 | 0.827 | 0.160 | 11 | 67487147 | stop gained | C/T | snv | 5 | |||
rs699473 | 0.827 | 0.160 | 4 | 24795181 | intron variant | C/T | snv | 0.54 | 5 | ||
rs121434259 | 0.925 | 0.160 | 22 | 29636805 | stop gained | C/T | snv | 2 | |||
rs730882035 | 0.807 | 0.200 | 3 | 10149805 | missense variant | G/A | snv | 7 | |||
rs2235544 | 0.742 | 0.240 | 1 | 53909897 | intron variant | C/A;T | snv | 0.53; 4.0E-06 | 14 | ||
rs3731249 | 0.683 | 0.320 | 9 | 21970917 | missense variant | C/A;G;T | snv | 2.1E-02 | 23 | ||
rs1800067 | 0.716 | 0.320 | 16 | 13935176 | missense variant | G/A | snv | 5.6E-02 | 5.3E-02 | 17 | |
rs150766139 | 0.742 | 0.320 | 16 | 2046238 | stop gained | G/A | snv | 1.4E-03 | 1.4E-03 | 13 | |
rs9420907 | 0.790 | 0.320 | 10 | 103916707 | intron variant | C/A;G | snv | 7 |