Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs74315452 | 0.732 | 0.160 | 21 | 31667356 | missense variant | T/C | snv | 12 | |||
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 | ||
rs363371 | 0.882 | 0.120 | 10 | 117226885 | TF binding site variant | G/A | snv | 0.19 | 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 | ||
rs1159805691 | 0.851 | 0.080 | 16 | 1792266 | frameshift variant | T/- | del | 7.0E-06 | 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 |