Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 22 | |||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs9297976 | 0.790 | 0.160 | 8 | 142670817 | intron variant | T/C;G | snv | 7 | |||
rs12155758 | 0.882 | 0.080 | 8 | 142684467 | upstream gene variant | G/A | snv | 0.23 | 3 | ||
rs7855466 | 0.925 | 0.080 | 9 | 133245916 | downstream gene variant | C/T | snv | 0.23 | 3 | ||
rs2920283 | 0.925 | 0.040 | 8 | 142675619 | intron variant | T/C | snv | 0.44 | 2 | ||
rs9411471 | 1.000 | 0.040 | 9 | 133244704 | intergenic variant | G/A | snv | 0.27 | 2 | ||
rs9919007 | 1.000 | 0.040 | 9 | 133244140 | intergenic variant | C/T | snv | 0.27 | 2 | ||
rs10105842 | 1.000 | 0.040 | 8 | 142590254 | intergenic variant | C/T | snv | 0.15 | 1 | ||
rs1036385 | 1.000 | 0.040 | 8 | 142761483 | upstream gene variant | T/C;G | snv | 1 | |||
rs16896391 | 1.000 | 0.040 | 6 | 65196105 | intron variant | T/C | snv | 0.23 | 1 | ||
rs2164308 | 1.000 | 0.040 | 8 | 142704241 | 3 prime UTR variant | C/T | snv | 0.49 | 1 | ||
rs2572904 | 1.000 | 0.040 | 8 | 142710775 | intron variant | A/C | snv | 0.49 | 1 | ||
rs2585140 | 1.000 | 0.040 | 8 | 142725478 | intron variant | A/G | snv | 0.51 | 1 | ||
rs28473387 | 1.000 | 0.040 | 8 | 142626112 | intergenic variant | T/C | snv | 0.63 | 1 | ||
rs2920297 | 1.000 | 0.040 | 8 | 142681665 | 3 prime UTR variant | A/G | snv | 0.44 | 1 | ||
rs7046863 | 1.000 | 0.040 | 9 | 133246054 | downstream gene variant | T/C | snv | 0.27 | 1 | ||
rs7775478 | 1.000 | 0.040 | 6 | 65151300 | intron variant | G/T | snv | 0.26 | 1 | ||
rs9324593 | 1.000 | 0.040 | 8 | 142605634 | intergenic variant | A/G | snv | 0.18 | 1 | ||
rs975618 | 1.000 | 0.040 | 6 | 65114686 | intron variant | G/A | snv | 0.27 | 1 | ||
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs2976391 | 0.790 | 0.160 | 8 | 142681306 | intron variant | C/A;G | snv | 0.42; 2.5E-04 | 7 | ||
rs138377917 | 0.827 | 0.160 | 8 | 142682113 | stop gained | G/A | snv | 2.1E-02 | 2.2E-02 | 5 |