Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519753 | 0.763 | 0.120 | 1 | 64846664 | missense variant | C/A | snv | 9 | |||
rs1966862 | 0.790 | 0.120 | 4 | 85766908 | intron variant | A/G | snv | 0.14 | 8 | ||
rs10994982 | 0.790 | 0.120 | 10 | 61950345 | intron variant | A/G | snv | 0.49 | 7 | ||
rs121913488 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 7 | |||
rs869312821 | 0.882 | 0.120 | 1 | 1806515 | missense variant | T/C | snv | 7 | |||
rs924607 | 0.851 | 0.120 | 5 | 609978 | intron variant | C/T | snv | 0.32 | 7 | ||
rs1057519743 | 0.827 | 0.120 | Y | 1196852 | missense variant | A/C | snv | 6 | |||
rs2413739 | 0.827 | 0.120 | 22 | 43001030 | intron variant | C/T | snv | 0.43 | 6 | ||
rs387906517 | 0.827 | 0.120 | 9 | 130862919 | missense variant | G/A | snv | 6 | |||
rs724159947 | 0.851 | 0.120 | 12 | 11869601 | missense variant | C/T | snv | 6 | |||
rs9479 | 0.851 | 0.120 | 15 | 74036235 | 3 prime UTR variant | A/G | snv | 0.50 | 6 | ||
rs1057519866 | 0.851 | 0.120 | 10 | 103093198 | missense variant | C/T | snv | 5 | |||
rs121913448 | 0.827 | 0.120 | 9 | 130862976 | missense variant | G/A | snv | 5 | |||
rs6021191 | 0.851 | 0.120 | 20 | 51419700 | intron variant | A/T | snv | 4.9E-02 | 5 | ||
rs7853758 | 0.851 | 0.120 | 9 | 84286011 | synonymous variant | G/A | snv | 0.15 | 0.19 | 5 | |
rs869312953 | 0.851 | 0.120 | 1 | 64846735 | missense variant | G/T | snv | 5 | |||
rs17007695 | 0.851 | 0.120 | 4 | 141788570 | intergenic variant | T/C | snv | 7.7E-02 | 4 | ||
rs17069665 | 0.882 | 0.120 | 6 | 108620265 | intron variant | A/C;G | snv | 4 | |||
rs186364861 | 0.882 | 0.120 | 13 | 48037798 | missense variant | G/A | snv | 9.1E-04 | 2.4E-04 | 4 | |
rs2274407 | 0.882 | 0.120 | 13 | 95206781 | missense variant | C/A;G;T | snv | 9.7E-02 | 0.10 | 4 | |
rs4646450 | 0.882 | 0.120 | 7 | 99668695 | 3 prime UTR variant | G/A | snv | 0.38 | 4 | ||
rs4748793 | 0.851 | 0.120 | 10 | 22194082 | intergenic variant | A/G | snv | 0.18 | 4 | ||
rs6964969 | 0.851 | 0.120 | 7 | 50405553 | downstream gene variant | A/G | snv | 0.23 | 4 | ||
rs7088318 | 0.851 | 0.120 | 10 | 22564019 | intron variant | C/A | snv | 0.55 | 4 | ||
rs757874631 | 0.882 | 0.120 | 11 | 119278211 | missense variant | T/A;C | snv | 4 |