Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 27 | ||
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 21 | |
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 18 | ||
rs17145738 | 0.851 | 0.200 | 7 | 73568544 | 3 prime UTR variant | C/T | snv | 0.11 | 11 | ||
rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 9 | |||
rs2244608 | 0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 | 9 | ||
rs1051921 | 0.925 | 0.120 | 7 | 73593613 | 3 prime UTR variant | G/A | snv | 0.15 | 8 | ||
rs3741414 | 0.925 | 0.120 | 12 | 57450266 | 3 prime UTR variant | C/T | snv | 0.19 | 7 | ||
rs12423664 | 1.000 | 0.040 | 12 | 132493308 | intron variant | G/A | snv | 0.10 | 6 | ||
rs12801636 | 1.000 | 0.040 | 11 | 65623846 | intron variant | G/A | snv | 0.25 | 5 | ||
rs79598313 | 1 | 26958422 | intron variant | C/A;T | snv | 5 |