Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28998802 | 0.807 | 0.120 | 17 | 27797882 | intron variant | G/A | snv | 0.11 | 6 | ||
rs367569 | 0.807 | 0.120 | 16 | 11271643 | intron variant | C/T | snv | 0.32 | 6 | ||
rs4561177 | 0.807 | 0.120 | 11 | 110091706 | intron variant | A/G | snv | 0.36 | 6 | ||
rs9264942 | 0.763 | 0.400 | 6 | 31306603 | intron variant | T/C | snv | 0.34 | 5 | ||
rs1250544 | 0.882 | 0.080 | 10 | 79273128 | intron variant | G/A | snv | 0.32 | 3 | ||
rs1056198 | 0.925 | 0.040 | 20 | 49939692 | intron variant | C/T | snv | 0.34 | 2 | ||
rs17716942 | 0.925 | 0.040 | 2 | 162404181 | intron variant | T/C | snv | 9.6E-02 | 2 | ||
rs181359 | 0.882 | 0.080 | 22 | 21574352 | intron variant | G/A | snv | 0.21 | 2 | ||
rs2066819 | 0.925 | 0.040 | 12 | 56356420 | intron variant | C/T | snv | 4.9E-02 | 4.5E-02 | 2 | |
rs2675662 | 0.925 | 0.040 | 10 | 73839369 | intron variant | A/G | snv | 0.55 | 2 | ||
rs27432 | 0.925 | 0.040 | 5 | 96783569 | intron variant | A/C;G | snv | 2 | |||
rs4406273 | 0.925 | 0.040 | 6 | 31298313 | intron variant | G/A | snv | 8.6E-02 | 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 | ||
rs610604 | 0.827 | 0.240 | 6 | 137878280 | intron variant | G/T | snv | 0.58 | 2 | ||
rs62149416 | 0.925 | 0.040 | 2 | 60856371 | intron variant | T/C | snv | 0.26 | 2 | ||
rs7637230 | 0.925 | 0.040 | 3 | 101944711 | intron variant | A/G;T | snv | 2 | |||
rs7709212 | 0.925 | 0.040 | 5 | 159337169 | intron variant | T/C | snv | 0.34 | 2 | ||
rs892085 | 0.925 | 0.040 | 19 | 10707416 | intron variant | G/A | snv | 0.57 | 0.59 | 2 | |
rs12489120 | 1.000 | 0.040 | 3 | 4978778 | intron variant | C/A;G;T | snv | 1 | |||
rs27524 | 0.851 | 0.160 | 5 | 96766240 | intron variant | A/G | snv | 0.61 | 1 | ||
rs4712528 | 1.000 | 0.040 | 6 | 20678199 | intron variant | G/C;T | snv | 1 | |||
rs4722404 | 0.851 | 0.120 | 7 | 3089155 | intron variant | T/C | snv | 0.40 | 1 | ||
rs9394026 | 1.000 | 0.040 | 6 | 31014767 | intron variant | G/A | snv | 0.24 | 1 | ||
rs10865331 | 0.827 | 0.120 | 2 | 62324337 | intergenic variant | A/G | snv | 0.57 | 5 |