Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs387907272 | 0.572 | 0.520 | 3 | 38141150 | stop lost | T/C | snv | 5.2E-05 | 7.0E-06 | 73 | |
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs2104286 | 0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 | 25 | ||
rs6897932 | 0.683 | 0.560 | 5 | 35874473 | missense variant | C/T | snv | 0.23 | 0.21 | 25 | |
rs1065489 | 0.695 | 0.440 | 1 | 196740644 | missense variant | G/T | snv | 0.20 | 0.15 | 19 | |
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 19 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 14 | ||
rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 11 | |||
rs11209032 | 0.752 | 0.400 | 1 | 67274409 | upstream gene variant | G/A | snv | 0.30 | 10 | ||
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 10 | |
rs7421861 | 0.790 | 0.200 | 2 | 241853198 | intron variant | A/G;T | snv | 9 | |||
rs1048709 | 0.776 | 0.320 | 6 | 31947158 | synonymous variant | A/G | snv | 0.82 | 0.85 | 8 | |
rs2075800 | 0.776 | 0.440 | 6 | 31810169 | missense variant | C/T | snv | 0.32 | 0.25 | 8 | |
rs4505848 | 0.776 | 0.400 | 4 | 122211337 | intron variant | A/G | snv | 0.29 | 8 | ||
rs17375018 | 0.790 | 0.360 | 1 | 67189464 | intron variant | G/A | snv | 0.29 | 7 | ||
rs4788084 | 0.827 | 0.200 | 16 | 28528527 | downstream gene variant | C/T | snv | 0.36 | 6 | ||
rs1128334 | 0.851 | 0.160 | 11 | 128459064 | 3 prime UTR variant | C/T | snv | 0.11 | 5 | ||
rs2222202 | 0.827 | 0.160 | 1 | 206772036 | intron variant | G/A | snv | 0.39 | 5 | ||
rs10893872 | 0.882 | 0.120 | 11 | 128455658 | downstream gene variant | T/C | snv | 0.44 | 4 | ||
rs6841698 | 0.882 | 0.080 | 4 | 38760093 | upstream gene variant | G/A | snv | 0.36 | 4 | ||
rs12569232 | 0.882 | 0.280 | 1 | 211379722 | intron variant | G/C;T | snv | 4 | |||
rs703842 | 0.851 | 0.240 | 12 | 57768956 | missense variant | A/G | snv | 0.38 | 0.33 | 4 |