Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 11 | |||
rs7421861 | 0.790 | 0.200 | 2 | 241853198 | intron variant | A/G;T | snv | 9 | |||
rs10863888 | 0.851 | 0.280 | 1 | 211329427 | intron variant | A/C;G;T | snv | 4 | |||
rs12569232 | 0.882 | 0.280 | 1 | 211379722 | intron variant | G/C;T | snv | 4 | |||
rs104895462 | 0.882 | 0.120 | 16 | 50710911 | missense variant | C/T | snv | 3 | |||
rs397514601 | 0.882 | 0.040 | 11 | 77115423 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
rs7565639 | 0.882 | 0.160 | 2 | 241854911 | intron variant | T/A;C | snv | 3 | |||
rs104895460 | 0.925 | 0.080 | 16 | 50711316 | missense variant | C/T | snv | 2 | |||
rs7519847 | 1.000 | 0.040 | 1 | 22003194 | intron variant | C/G;T | snv | 1 | |||
rs387907272 | 0.572 | 0.520 | 3 | 38141150 | stop lost | T/C | snv | 5.2E-05 | 7.0E-06 | 73 | |
rs377679652 | 0.925 | 0.040 | 7 | 50669861 | missense variant | C/T | snv | 4.6E-05 | 2.8E-05 | 2 | |
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
rs2358820 | 1.000 | 0.040 | 1 | 117169289 | intron variant | G/A | snv | 5.3E-02 | 1 | ||
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 10 | |
rs61860052 | 0.925 | 0.080 | 10 | 80201955 | intron variant | C/A | snv | 6.4E-02 | 2 | ||
rs4752 | 1.000 | 0.040 | 4 | 71756849 | synonymous variant | A/G | snv | 3.8E-02 | 8.6E-02 | 1 | |
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs12722489 | 0.882 | 0.160 | 10 | 6060049 | intron variant | C/T | snv | 0.11 | 3 | ||
rs1128334 | 0.851 | 0.160 | 11 | 128459064 | 3 prime UTR variant | C/T | snv | 0.11 | 5 | ||
rs1040461 | 1.000 | 0.040 | 6 | 57190556 | missense variant | C/T | snv | 9.8E-02 | 0.12 | 1 | |
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 14 | ||
rs1805110 | 0.882 | 0.200 | 1 | 91861488 | missense variant | G/A | snv | 0.13 | 0.13 | 3 | |
rs1065489 | 0.695 | 0.440 | 1 | 196740644 | missense variant | G/T | snv | 0.20 | 0.15 | 19 | |
rs2287987 | 0.882 | 0.120 | 5 | 96793832 | missense variant | T/C | snv | 0.15 | 0.16 | 3 | |
rs2104286 | 0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 | 25 |