Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 17 | ||
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 16 | ||
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 10 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 9 | ||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 8 | |||
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 8 | |||
rs2571445 | 0.925 | 0.080 | 2 | 217818431 | missense variant | A/G;T | snv | 0.62 | 8 | ||
rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 7 | ||
rs55781567 | 0.851 | 0.080 | 15 | 78565644 | 5 prime UTR variant | C/G | snv | 0.31 | 7 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 6 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 6 | |
rs10922109 | 0.827 | 0.080 | 1 | 196735502 | intron variant | C/A | snv | 0.46 | 6 | ||
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 6 | |
rs9788721 | 1.000 | 0.040 | 15 | 78510527 | intron variant | C/T | snv | 0.65 | 6 | ||
rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 6 | ||
rs2853677 | 0.724 | 0.240 | 5 | 1287079 | 3 prime UTR variant | G/A | snv | 0.63 | 6 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 5 | ||
rs7655625 | 1.000 | 0.040 | 4 | 144564763 | intron variant | T/C;G | snv | 5 | |||
rs1410996 | 0.807 | 0.240 | 1 | 196727803 | intron variant | G/A | snv | 0.46 | 5 | ||
rs138544659 | 1.000 | 0.040 | 15 | 78608359 | intron variant | T/G | snv | 0.28 | 5 | ||
rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 5 | |
rs190065944 | 0.925 | 0.080 | 15 | 78567268 | intron variant | G/A | snv | 3.4E-03 | 5 | ||
rs55958997 | 1.000 | 0.040 | 15 | 78623530 | upstream gene variant | C/A | snv | 0.32 | 5 |