Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397508687 | 0.827 | 0.080 | 7 | 117531040 | frameshift variant | -/GA | ins | 4.0E-06 | 5 | ||
rs2647087 | 1.000 | 0.040 | 6 | 32713272 | upstream gene variant | A/C | snv | 0.29 | 2 | ||
rs76371115 | 0.807 | 0.160 | 7 | 117531041 | missense variant | A/C;G;T | snv | 8.0E-06 | 6 | ||
rs111033566 | 0.742 | 0.280 | 7 | 142750600 | missense variant | A/C;T | snv | 11 | |||
rs1223231582 | 0.677 | 0.280 | 7 | 142750639 | missense variant | A/G | snv | 7.0E-06 | 24 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs777418530 | 0.763 | 0.120 | 16 | 84845883 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 10 | |
rs111033567 | 0.882 | 0.040 | 7 | 142750582 | missense variant | A/G | snv | 3 | |||
rs397507442 | 0.925 | 0.040 | 7 | 142750579 | missense variant | A/G | snv | 2 | |||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs57749775 | 0.851 | 0.080 | 12 | 52904822 | missense variant | A/G;T | snv | 1.7E-03; 4.0E-06 | 6 | ||
rs12008279 | 0.882 | 0.080 | X | 106917472 | intron variant | A/G;T | snv | 3 | |||
rs886037775 | 0.882 | 0.120 | 8 | 19960948 | missense variant | A/T | snv | 7 | |||
rs62561366 | 1.000 | 0.040 | 9 | 95555669 | intergenic variant | A/T | snv | 3.9E-02 | 2 | ||
rs11554495 | 0.701 | 0.240 | 12 | 52904798 | missense variant | C/A | snv | 4.9E-03 | 5.4E-03 | 19 | |
rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
rs756322971 | 0.763 | 0.240 | 3 | 122284955 | missense variant | C/A;G | snv | 9 | |||
rs387906698 | 0.827 | 0.040 | 7 | 142751919 | missense variant | C/A;T | snv | 4.0E-06; 7.2E-05 | 8 | ||
rs5917027 | 1.000 | 0.040 | X | 106919404 | intron variant | C/A;T | snv | 1 | |||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
rs118204082 | 0.851 | 0.120 | 8 | 19955863 | missense variant | C/G;T | snv | 1.5E-04 | 4 | ||
rs111033568 | 0.882 | 0.040 | 7 | 142751937 | missense variant | C/G;T | snv | 2.0E-05 | 3 | ||
rs772223589 | 0.925 | 0.120 | 7 | 117590391 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 3 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 |