Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7552167 | 0.807 | 0.120 | 1 | 24192153 | upstream gene variant | A/G | snv | 0.87 | 6 | ||
rs9988642 | 0.882 | 0.080 | 1 | 67260421 | downstream gene variant | T/C | snv | 0.13 | 3 | ||
rs7536201 | 0.925 | 0.040 | 1 | 24966593 | upstream gene variant | T/C;G | snv | 2 | |||
rs4649203 | 0.851 | 0.160 | 1 | 24193430 | intergenic variant | G/A | snv | 0.61 | 1 | ||
rs4845454 | 0.925 | 0.040 | 1 | 152619708 | downstream gene variant | C/A;T | snv | 1 | |||
rs10865331 | 0.827 | 0.120 | 2 | 62324337 | intergenic variant | A/G | snv | 0.57 | 5 | ||
rs17716942 | 0.925 | 0.040 | 2 | 162404181 | intron variant | T/C | snv | 9.6E-02 | 2 | ||
rs62149416 | 0.925 | 0.040 | 2 | 60856371 | intron variant | T/C | snv | 0.26 | 2 | ||
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 2 | |
rs4683946 | 0.925 | 0.080 | 3 | 101896982 | intron variant | G/T | snv | 0.19 | 2 | ||
rs4685408 | 0.925 | 0.040 | 3 | 16954543 | intron variant | G/A | snv | 0.56 | 2 | ||
rs7637230 | 0.925 | 0.040 | 3 | 101944711 | intron variant | A/G;T | snv | 2 | |||
rs12489120 | 1.000 | 0.040 | 3 | 4978778 | intron variant | C/A;G;T | snv | 1 | |||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 4 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 4 | |
rs17728338 | 0.851 | 0.160 | 5 | 151098757 | downstream gene variant | G/A | snv | 7.1E-02 | 2 | ||
rs2233278 | 0.925 | 0.040 | 5 | 151087628 | 5 prime UTR variant | G/C;T | snv | 4.8E-02 | 2 | ||
rs27432 | 0.925 | 0.040 | 5 | 96783569 | intron variant | A/C;G | snv | 2 | |||
rs7709212 | 0.925 | 0.040 | 5 | 159337169 | intron variant | T/C | snv | 0.34 | 2 | ||
rs27524 | 0.851 | 0.160 | 5 | 96766240 | intron variant | A/G | snv | 0.61 | 1 | ||
rs30187 | 0.732 | 0.360 | 5 | 96788627 | missense variant | T/A;C | snv | 0.62 | 1 | ||
rs2395029 | 0.790 | 0.320 | 6 | 31464003 | non coding transcript exon variant | T/G | snv | 2.7E-02 | 2.4E-02 | 7 | |
rs9264942 | 0.763 | 0.400 | 6 | 31306603 | intron variant | T/C | snv | 0.34 | 5 | ||
rs33980500 | 0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 | 3 | |
rs4406273 | 0.925 | 0.040 | 6 | 31298313 | intron variant | G/A | snv | 8.6E-02 | 2 |