Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 9 | |||
rs12608932 | 0.827 | 0.080 | 19 | 17641880 | intron variant | A/C | snv | 0.36 | 5 | ||
rs139550538 | 0.827 | 0.080 | 10 | 92524312 | intron variant | T/A | snv | 1.9E-02 | 5 | ||
rs2412208 | 0.827 | 0.080 | 1 | 7032722 | intron variant | T/G | snv | 0.33 | 5 | ||
rs34517613 | 0.827 | 0.080 | 17 | 28283226 | intron variant | C/T | snv | 9.1E-02 | 5 | ||
rs35714695 | 0.827 | 0.080 | 17 | 28392769 | intron variant | G/A;T | snv | 0.12 | 5 | ||
rs3849943 | 0.827 | 0.080 | 9 | 27543384 | non coding transcript exon variant | C/G;T | snv | 5 | |||
rs616147 | 0.827 | 0.080 | 3 | 39492990 | intron variant | A/G | snv | 0.76 | 5 | ||
rs1002442 | 0.851 | 0.080 | 10 | 60043304 | non coding transcript exon variant | T/G | snv | 0.14 | 4 | ||
rs10029851 | 0.851 | 0.080 | 4 | 108706869 | intergenic variant | A/C;T | snv | 4 | |||
rs10145110 | 0.851 | 0.080 | 14 | 101008533 | intron variant | C/T | snv | 9.7E-02 | 4 | ||
rs11061269 | 0.851 | 0.080 | 12 | 130971904 | intron variant | G/A | snv | 7.5E-02 | 4 | ||
rs115134572 | 0.851 | 0.080 | 3 | 143629403 | intron variant | A/G | snv | 2.0E-02 | 4 | ||
rs11590421 | 0.851 | 0.080 | 1 | 38528443 | intergenic variant | G/A | snv | 0.15 | 4 | ||
rs11744876 | 0.851 | 0.080 | 5 | 11084600 | intron variant | G/A | snv | 7.8E-02 | 4 | ||
rs11987758 | 0.851 | 0.080 | 8 | 2180583 | regulatory region variant | G/A | snv | 0.12 | 4 | ||
rs12891047 | 0.851 | 0.080 | 14 | 67776358 | intron variant | C/A | snv | 0.62 | 4 | ||
rs13100616 | 0.851 | 0.080 | 3 | 178681763 | intron variant | A/G | snv | 0.33 | 4 | ||
rs1400816 | 0.851 | 0.080 | 2 | 171824168 | intron variant | A/C | snv | 0.81 | 4 | ||
rs1464443 | 0.851 | 0.080 | 2 | 212050001 | intron variant | C/A;T | snv | 4 | |||
rs1559473 | 0.851 | 0.080 | 2 | 222016799 | intergenic variant | T/G | snv | 0.25 | 4 | ||
rs1605070 | 0.851 | 0.080 | 3 | 51882999 | intergenic variant | C/A | snv | 0.60 | 4 | ||
rs16938145 | 0.851 | 0.080 | 9 | 2256092 | intergenic variant | T/C;G | snv | 4 | |||
rs16975050 | 0.851 | 0.080 | 18 | 41607206 | intron variant | T/G | snv | 7.0E-02 | 4 | ||
rs17162257 | 0.851 | 0.080 | 1 | 26602511 | upstream gene variant | T/A;G | snv | 4 |