Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs1258159645 | 0.630 | 0.600 | 16 | 69711128 | missense variant | G/A | snv | 7.0E-06 | 37 | ||
rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 | |
rs6314 | 0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 | 23 | |
rs1065852 | 0.695 | 0.360 | 22 | 42130692 | missense variant | G/A | snv | 0.21 | 0.19 | 19 | |
rs995922697 | 0.724 | 0.560 | 3 | 49357413 | missense variant | A/G | snv | 4.1E-06 | 15 | ||
rs10828317 | 0.776 | 0.280 | 10 | 22550699 | missense variant | T/C | snv | 9 | |||
rs1322643228 | 0.807 | 0.280 | 12 | 104321110 | missense variant | C/T | snv | 7.1E-06 | 6 | ||
rs781598341 | 0.827 | 0.240 | 6 | 159682510 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
rs1182593032 | 0.851 | 0.200 | 16 | 69718516 | missense variant | A/G | snv | 4 | |||
rs1231813088 | 0.851 | 0.160 | 10 | 92690015 | missense variant | C/T | snv | 4 | |||
rs1322425552 | 0.851 | 0.160 | 17 | 74923048 | missense variant | G/A | snv | 4 | |||
rs1457049406 | 0.851 | 0.200 | 22 | 19962555 | missense variant | C/T | snv | 4 | |||
rs1330075052 | 0.882 | 0.160 | 12 | 104215828 | missense variant | T/C | snv | 1.4E-05 | 3 | ||
rs201934979 | 0.882 | 0.160 | 15 | 74749838 | missense variant | C/T | snv | 8.8E-05; 8.0E-06 | 1.3E-04 | 3 | |
rs2230469 | 0.882 | 0.160 | 10 | 22550699 | missense variant | T/C | snv | 0.27 | 0.24 | 3 | |
rs1447119000 | 0.925 | 0.120 | 22 | 42130763 | missense variant | G/A | snv | 2 | |||
rs767413934 | 0.925 | 0.120 | 11 | 113424539 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs3755557 | 0.807 | 0.280 | 3 | 120096110 | non coding transcript exon variant | T/A | snv | 0.14 | 6 | ||
rs905568 | 0.925 | 0.120 | 3 | 114232449 | non coding transcript exon variant | C/A;G;T | snv | 2 | |||
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
rs6277 | 0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 | 36 |