Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs59758982 | 0.925 | 0.040 | 17 | 7676326 | intron variant | TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC/-;TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC | delins | 0.82 | 2 | ||
rs1641549 | 17 | 7671457 | intron variant | C/T | snv | 0.35 | 1 | ||||
rs8064946 | 0.851 | 0.080 | 17 | 7685993 | non coding transcript exon variant | G/C | snv | 0.32 | 4 | ||
rs2287497 | 0.882 | 0.120 | 17 | 7689462 | intron variant | G/A | snv | 0.25 | 3 | ||
rs35119871 | 17 | 7664197 | intron variant | C/T | snv | 0.22 | 1 | ||||
rs75821853 | 1.000 | 0.080 | 17 | 7675397 | 5 prime UTR variant | T/C | snv | 0.18 | 1 | ||
rs12602273 | 0.851 | 0.080 | 17 | 7679695 | intron variant | C/G | snv | 0.15 | 4 | ||
rs2287498 | 0.882 | 0.120 | 17 | 7689242 | synonymous variant | C/T | snv | 0.13 | 0.14 | 4 | |
rs12951053 | 0.732 | 0.160 | 17 | 7674089 | intron variant | A/C | snv | 0.10 | 14 | ||
rs12947788 | 0.776 | 0.280 | 17 | 7674109 | intron variant | G/A | snv | 0.10 | 8 | ||
rs9895829 | 0.807 | 0.080 | 17 | 7675361 | 5 prime UTR variant | A/G | snv | 7.4E-02 | 6 | ||
rs8079544 | 1.000 | 0.040 | 17 | 7676734 | intron variant | C/T | snv | 7.4E-02 | 2 | ||
rs17884306 | 0.925 | 0.120 | 17 | 7668783 | 3 prime UTR variant | C/T | snv | 5.1E-02 | 2 | ||
rs8078476 | 17 | 7677910 | intron variant | G/A | snv | 4.6E-02 | 2 | ||||
rs35850753 | 0.807 | 0.080 | 17 | 7675353 | 5 prime UTR variant | C/T | snv | 1.3E-02 | 8 | ||
rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 37 | ||
rs35117667 | 1.000 | 17 | 7676278 | splice region variant | G/A | snv | 2.1E-03 | 8.3E-03 | 1 | ||
rs55819519 | 0.627 | 0.400 | 17 | 7673751 | missense variant | C/A;G;T | snv | 1.6E-04 | 1.3E-04 | 40 | |
rs143458271 | 0.925 | 0.080 | 17 | 7676589 | synonymous variant | C/T | snv | 9.2E-05 | 8.4E-05 | 2 | |
rs72661120 | 17 | 7673717 | synonymous variant | T/C | snv | 2.7E-04 | 7.0E-05 | 1 | |||
rs770374782 | 0.851 | 0.160 | 17 | 7673752 | missense variant | G/A;C | snv | 1.2E-05 | 4.2E-05 | 6 | |
rs764562217 | 0.882 | 0.120 | 17 | 7673308 | stop lost | T/G | snv | 2.3E-05 | 3.5E-05 | 3 | |
rs573154688 | 1.000 | 0.160 | 17 | 7670711 | missense variant | C/T | snv | 4.4E-05 | 3.5E-05 | 3 | |
rs137852789 | 0.925 | 0.080 | 17 | 7675152 | missense variant | C/G;T | snv | 4.0E-06 | 3.5E-05 | 3 | |
rs371524413 | 0.925 | 0.200 | 17 | 7675145 | missense variant | C/G;T | snv | 1.6E-05 | 2.8E-05 | 3 |