Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7890572 | X | 29622701 | intron variant | A/G | snv | 9.3E-02 | 5 | ||||
rs5942937 | X | 110473179 | intron variant | T/G | snv | 0.47 | 4 | ||||
rs5985471 | X | 110460733 | downstream gene variant | C/T | snv | 0.43 | 4 | ||||
rs138331350 | X | 14841981 | intron variant | G/A | snv | 3.7E-02 | 1 | ||||
rs2294915 | 1.000 | 0.040 | 22 | 43945024 | intron variant | C/G;T | snv | 5 | |||
rs1811069 | 1.000 | 0.040 | 22 | 21627765 | upstream gene variant | T/A;G | snv | 4 | |||
rs4820323 | 22 | 38203760 | non coding transcript exon variant | C/A;G;T | snv | 4 | |||||
rs133027 | 22 | 38179492 | intron variant | T/- | delins | 0.46 | 2 | ||||
rs181362 | 22 | 21577779 | intron variant | C/T | snv | 0.31 | 2 | ||||
rs4821116 | 0.925 | 0.120 | 22 | 21619030 | intron variant | C/A;T | snv | 0.18 | 2 | ||
rs5754166 | 0.925 | 0.160 | 22 | 21576488 | intron variant | C/T | snv | 0.18 | 2 | ||
rs7444 | 1.000 | 0.080 | 22 | 21622645 | 3 prime UTR variant | T/C | snv | 0.32 | 2 | ||
rs7445 | 22 | 21622758 | 3 prime UTR variant | C/G;T | snv | 0.22 | 2 | ||||
rs147122512 | 22 | 40394561 | intron variant | G/A;C | snv | 1 | |||||
rs181360 | 22 | 21574627 | intron variant | T/G | snv | 0.21 | 1 | ||||
rs2899297 | 22 | 38198661 | intron variant | G/A | snv | 0.52 | 1 | ||||
rs372767202 | 22 | 35363972 | intergenic variant | T/C | snv | 4.2E-05 | 1 | ||||
rs5754344 | 1.000 | 0.080 | 22 | 21609497 | intron variant | A/G | snv | 0.18 | 1 | ||
rs8135828 | 22 | 29533250 | intron variant | G/A | snv | 0.14 | 1 | ||||
rs8142788 | 22 | 29004527 | intron variant | G/A | snv | 0.11 | 1 | ||||
rs235314 | 21 | 44851537 | missense variant | C/T | snv | 0.48 | 0.46 | 3 | |||
rs496300 | 1.000 | 0.040 | 21 | 43359800 | intron variant | C/T | snv | 0.73 | 2 | ||
rs235374 | 21 | 44875071 | upstream gene variant | G/C | snv | 0.39 | 1 | ||||
rs2834707 | 21 | 34971255 | intron variant | C/T | snv | 0.35 | 1 | ||||
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 17 |