Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs71559680 | 0.827 | 0.120 | 6 | 21430497 | intergenic variant | TAG/CAT | mnv | 6 | |||
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
rs3212227 | 0.566 | 0.840 | 5 | 159315942 | 3 prime UTR variant | T/G | snv | 0.26 | 65 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 19 | ||
rs2395029 | 0.790 | 0.320 | 6 | 31464003 | non coding transcript exon variant | T/G | snv | 2.7E-02 | 2.4E-02 | 12 | |
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 10 | |
rs1569414 | 0.807 | 0.160 | 22 | 45331684 | intron variant | T/G | snv | 0.44 | 6 | ||
rs34779708 | 0.827 | 0.120 | 10 | 35177257 | intron variant | T/G | snv | 0.33 | 6 | ||
rs3776414 | 0.827 | 0.120 | 5 | 10689450 | intron variant | T/G | snv | 0.48 | 6 | ||
rs4243971 | 0.827 | 0.120 | 20 | 32261714 | intergenic variant | T/G | snv | 0.64 | 6 | ||
rs111305875 | 0.827 | 0.120 | 6 | 167098098 | intron variant | T/G | snv | 3.0E-02 | 5 | ||
rs12987977 | 0.827 | 0.120 | 2 | 102358876 | intron variant | T/G | snv | 0.31 | 5 | ||
rs4085613 | 0.827 | 0.160 | 1 | 152577542 | downstream gene variant | T/G | snv | 0.59 | 5 | ||
rs6425143 | 0.827 | 0.120 | 1 | 172875212 | intron variant | T/G | snv | 0.34 | 5 | ||
rs130067 | 0.851 | 0.200 | 6 | 31150734 | missense variant | T/G | snv | 0.23 | 0.21 | 4 | |
rs3134792 | 0.851 | 0.280 | 6 | 31344549 | intron variant | T/G | snv | 8.8E-02 | 4 | ||
rs10789285 | 1.000 | 0.040 | 1 | 69322799 | intergenic variant | T/G | snv | 0.33 | 2 | ||
rs8016947 | 0.925 | 0.080 | 14 | 35363460 | intron variant | T/G | snv | 0.60 | 2 | ||
rs12972990 | 1.000 | 0.040 | 19 | 10295755 | intron variant | T/G | snv | 0.35 | 1 | ||
rs771797724 | 1.000 | 0.040 | 10 | 14908688 | missense variant | T/G | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 |