Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs121913682 | 0.605 | 0.400 | 4 | 54733167 | missense variant | A/G;T | snv | 52 | |||
rs121913507 | 0.614 | 0.400 | 4 | 54733155 | missense variant | A/T | snv | 49 | |||
rs147001633 | 0.776 | 0.240 | 2 | 25234373 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.2E-04 | 15 | ||
rs4740 | 0.827 | 0.240 | 19 | 4236999 | missense variant | G/A | snv | 0.34 | 0.39 | 8 | |
rs5754217 | 0.925 | 0.120 | 22 | 21585386 | intron variant | G/T | snv | 0.31 | 7 | ||
rs3093030 | 0.925 | 0.120 | 19 | 10286727 | non coding transcript exon variant | C/T | snv | 0.34 | 6 | ||
rs1639150 | 0.925 | 0.120 | 16 | 3697203 | intron variant | C/T | snv | 0.49 | 3 | ||
rs2072379 | 0.925 | 0.120 | 16 | 3688886 | intron variant | C/T | snv | 0.75 | 3 | ||
rs6983130 | 1.000 | 0.080 | 8 | 55880680 | intron variant | A/G | snv | 0.18 | 2 | ||
rs981505482 | 1.000 | 0.120 | 1 | 155294506 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 2 | |
rs12597773 | 1.000 | 0.040 | 16 | 3714708 | intron variant | G/A;C | snv | 2 | |||
rs3751842 | 1.000 | 0.040 | 16 | 3664610 | 3 prime UTR variant | C/G;T | snv | 2 |