Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800682 | 0.637 | 0.440 | 10 | 88990206 | non coding transcript exon variant | A/G | snv | 0.54 | 32 | ||
rs752626029 | 0.925 | 0.120 | 2 | 25239208 | missense variant | G/A;C;T | snv | 4.0E-06; 1.2E-05; 4.0E-06 | 2 | ||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs759834538 | 0.925 | 0.120 | 9 | 136517294 | missense variant | C/A | snv | 1.7E-05 | 3 | ||
rs572432356 | 0.925 | 0.120 | 5 | 75596681 | missense variant | A/C | snv | 2 | |||
rs35631544 | 0.925 | 0.120 | 16 | 24191130 | missense variant | C/A;G | snv | 6.3E-04 | 1.0E-03 | 2 | |
rs72963007 | 1.000 | 0.120 | 4 | 105243566 | splice region variant | G/A | snv | 3.2E-03 | 1.0E-02 | 1 | |
rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 78 | ||
rs587781386 | 0.882 | 0.120 | 17 | 7674889 | missense variant | A/C;G | snv | 3.2E-05; 4.0E-06 | 3 | ||
rs764562217 | 0.882 | 0.120 | 17 | 7673308 | stop lost | T/G | snv | 2.3E-05 | 3.5E-05 | 3 | |
rs1157200929 | 0.925 | 0.120 | 19 | 22180315 | stop gained | T/A | snv | 2 |