Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 10 | ||
rs2230199 | 0.763 | 0.240 | 19 | 6718376 | missense variant | G/C;T | snv | 0.15 | 10 | ||
rs61755792 | 0.763 | 0.160 | 6 | 42721821 | missense variant | G/A;C | snv | 10 | |||
rs9332739 | 0.763 | 0.360 | 6 | 31936027 | missense variant | G/A;C | snv | 4.1E-06; 3.9E-02 | 10 | ||
rs641153 | 0.790 | 0.160 | 6 | 31946403 | missense variant | G/A;T | snv | 9.6E-02; 4.1E-06 | 7 | ||
rs121918567 | 0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 | 6 | ||
rs61755793 | 0.807 | 0.080 | 6 | 42721820 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs79037040 | 0.807 | 0.160 | 8 | 23225458 | non coding transcript exon variant | G/A;C;T | snv | 6 | |||
rs114254831 | 0.827 | 0.040 | 6 | 32187804 | intron variant | A/G | snv | 5 | |||
rs116503776 | 0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv | 5 | |||
rs148060787 | 0.851 | 0.080 | 11 | 61962853 | missense variant | C/G;T | snv | 4.4E-04 | 5 | ||
rs1626340 | 0.827 | 0.120 | 9 | 99161090 | intergenic variant | G/A;T | snv | 5 | |||
rs1800995 | 0.851 | 0.080 | 11 | 61955906 | missense variant | GC/AA | mnv | 5 | |||
rs1805142 | 0.851 | 0.080 | 11 | 61955825 | stop gained | G/C;T | snv | 2.7E-05 | 5 | ||
rs281865275 | 0.851 | 0.080 | 11 | 61957397 | missense variant | C/G;T | snv | 8.0E-06; 2.8E-05 | 5 | ||
rs61941274 | 0.827 | 0.160 | 12 | 111694806 | intron variant | G/A;T | snv | 5 | |||
rs62358361 | 0.851 | 0.040 | 5 | 39327786 | intron variant | G/C;T | snv | 5 | |||
rs73036519 | 0.851 | 0.040 | 19 | 45245104 | intron variant | G/A;C | snv | 5 | |||
rs114092250 | 0.851 | 0.040 | 5 | 35494346 | intergenic variant | G/A;T | snv | 4 | |||
rs11884770 | 0.851 | 0.040 | 2 | 227222204 | intron variant | T/A;C | snv | 4 | |||
rs181705462 | 0.851 | 0.040 | 6 | 31979250 | intron variant | G/C;T | snv | 4 | |||
rs55975637 | 0.851 | 0.040 | 3 | 99701009 | intron variant | G/A;T | snv | 4 | |||
rs5817082 | 0.851 | 0.040 | 16 | 56963437 | intron variant | -/A | delins | 4 | |||
rs71507014 | 0.851 | 0.040 | 9 | 70823689 | intron variant | -/C;CC | delins | 4 |