Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs502652 | 1.000 | 0.040 | 5 | 101043608 | intergenic variant | C/T | snv | 0.27 | 1 | ||
rs11191392 | 1.000 | 0.040 | 10 | 102767194 | intron variant | C/A | snv | 0.49 | 1 | ||
rs3740397 | 1.000 | 0.040 | 10 | 102832918 | 3 prime UTR variant | G/C | snv | 0.35 | 1 | ||
rs12765002 | 1.000 | 0.040 | 10 | 102875591 | intron variant | C/T | snv | 0.24 | 2 | ||
rs3740393 | 0.776 | 0.280 | 10 | 102876898 | intron variant | G/C;T | snv | 1 | |||
rs12260436 | 1.000 | 0.040 | 10 | 102981357 | intron variant | A/C | snv | 0.29 | 1 | ||
rs1890184 | 1.000 | 0.040 | 10 | 102988702 | intron variant | A/C;T | snv | 1 | |||
rs77420391 | 1.000 | 0.040 | 10 | 103186066 | intron variant | G/A | snv | 8.9E-02 | 2 | ||
rs246914 | 1.000 | 0.040 | 5 | 103223706 | intergenic variant | T/C | snv | 0.17 | 1 | ||
rs1163085 | 1.000 | 0.040 | 10 | 103279484 | intron variant | G/A | snv | 0.64 | 1 | ||
rs391236 | 1.000 | 0.040 | 5 | 103342372 | intergenic variant | A/G | snv | 0.24 | 1 | ||
rs2672852 | 1.000 | 0.040 | 2 | 103455652 | intergenic variant | C/T | snv | 0.44 | 1 | ||
rs4526367 | 1.000 | 0.040 | 8 | 10355952 | intron variant | G/A | snv | 0.77 | 1 | ||
rs10034259 | 1.000 | 0.040 | 4 | 104012596 | intron variant | A/C | snv | 0.19 | 1 | ||
rs150491901 | 1.000 | 0.040 | 8 | 10468395 | intergenic variant | G/A;T | snv | 1 | |||
rs1562927768 | 0.790 | 0.080 | 7 | 105101476 | frameshift variant | AAAGA/- | delins | 15 | |||
rs1826787 | 1.000 | 0.040 | 10 | 105908635 | downstream gene variant | C/T | snv | 0.16 | 1 | ||
rs1426371 | 1.000 | 0.040 | 12 | 108236003 | intron variant | G/A | snv | 0.20 | 3 | ||
rs3742020 | 1.000 | 0.040 | 12 | 109445449 | non coding transcript exon variant | T/C | snv | 0.33 | 1 | ||
rs10850379 | 1.000 | 0.040 | 12 | 109564972 | non coding transcript exon variant | C/T | snv | 0.40 | 1 | ||
rs11669576 | 0.851 | 0.160 | 19 | 11111624 | missense variant | G/A | snv | 4.3E-02 | 8.4E-02 | 1 | |
rs1143634 | 0.597 | 0.680 | 2 | 112832813 | synonymous variant | G/A | snv | 0.19 | 0.19 | 1 | |
rs4937872 | 1.000 | 0.040 | 11 | 112956992 | upstream gene variant | A/G;T | snv | 1 | |||
rs4245150 | 1.000 | 0.040 | 11 | 113493925 | intergenic variant | G/T | snv | 0.72 | 1 | ||
rs62551581 | 1.000 | 0.040 | 9 | 11610677 | intergenic variant | A/C | snv | 0.15 | 1 |