Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3219466 | 0.851 | 0.080 | 1 | 45340381 | 5 prime UTR variant | G/A;T | snv | 4 | |||
rs10936599 | 0.637 | 0.600 | 3 | 169774313 | synonymous variant | C/T | snv | 0.29 | 0.21 | 32 | |
rs1805794 | 0.605 | 0.600 | 8 | 89978251 | missense variant | C/G | snv | 0.35 | 0.31 | 41 | |
rs121434259 | 0.925 | 0.160 | 22 | 29636805 | stop gained | C/T | snv | 2 | |||
rs587776563 | 1.000 | 0.080 | 22 | 29668440 | frameshift variant | A/- | delins | 1 | |||
rs150766139 | 0.742 | 0.320 | 16 | 2046238 | stop gained | G/A | snv | 1.4E-03 | 1.4E-03 | 13 | |
rs25406 | 0.807 | 0.120 | 20 | 5118990 | intron variant | G/A | snv | 0.41 | 8 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs121918347 | 0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv | 4 | |||
rs699473 | 0.827 | 0.160 | 4 | 24795181 | intron variant | C/T | snv | 0.54 | 5 | ||
rs9420907 | 0.790 | 0.320 | 10 | 103916707 | intron variant | C/A;G | snv | 7 | |||
rs202247756 | 1.000 | 0.080 | 10 | 102550019 | missense variant | C/T | snv | 2 | |||
rs2736100 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 83 | ||
rs768803947 | 0.882 | 0.080 | 17 | 7670624 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs730882035 | 0.807 | 0.200 | 3 | 10149805 | missense variant | G/A | snv | 7 | |||
rs7574920 | 0.882 | 0.080 | 2 | 31362783 | intron variant | G/C | snv | 0.42 | 3 | ||
rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 |