Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10033366 | 4 | 110409934 | intron variant | T/C | snv | 0.92 | 1 | ||||
rs10033464 | 0.807 | 0.200 | 4 | 110799605 | downstream gene variant | T/G | snv | 0.86 | 1 | ||
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 8 | |
rs10050860 | 0.882 | 0.240 | 5 | 96786506 | missense variant | C/T | snv | 0.15 | 0.16 | 1 | |
rs10069554 | 5 | 33204354 | intron variant | T/C | snv | 0.45 | 1 | ||||
rs10184428 | 2 | 164155317 | intron variant | C/A;G | snv | 5 | |||||
rs10188442 | 2 | 132431666 | intron variant | C/T | snv | 0.22 | 1 | ||||
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 10 | ||
rs1027989 | 8 | 55901862 | intron variant | G/A;C | snv | 3 | |||||
rs10279895 | 7 | 27288591 | intergenic variant | A/G | snv | 2.9E-02 | 1 | ||||
rs104886142 | 0.790 | 0.280 | X | 108598793 | missense variant | G/A | snv | 8.7E-05 | 4.7E-05 | 4 | |
rs104893831 | 0.925 | 0.040 | 3 | 10146549 | missense variant | G/A;C;T | snv | 2.0E-05 | 2 | ||
rs104893914 | 1.000 | 0.080 | 5 | 143282714 | missense variant | C/T | snv | 1 | |||
rs104894145 | 0.925 | 0.240 | 10 | 102830946 | missense variant | G/A | snv | 1 | |||
rs10496288 | 2 | 83065441 | intergenic variant | T/C | snv | 0.13 | 1 | ||||
rs10496289 | 2 | 83066256 | intergenic variant | C/T | snv | 0.13 | 1 | ||||
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 11 | |
rs1057518797 | 4 | 88008090 | frameshift variant | CCCGGGCA/TAGGACG | delins | 3 | |||||
rs1057518856 | 0.882 | 0.240 | 16 | 2102397 | missense variant | A/T | snv | 5 | |||
rs1057518897 | 0.925 | 0.120 | 16 | 2103746 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
rs1057518899 | 16 | 2111647 | stop gained | G/A | snv | 2 | |||||
rs1057518903 | 0.882 | 0.160 | 11 | 64807890 | splice region variant | C/- | delins | 6 | |||
rs1057518959 | 16 | 2091794 | missense variant | A/G | snv | 2 | |||||
rs1057523354 | 0.763 | 0.480 | 13 | 110179387 | missense variant | C/A | snv | 13 | |||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 7 |