Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs3828805 | 0.752 | 0.160 | 6 | 32668343 | 5 prime UTR variant | T/A;C | snv | 12 | |||
rs1453414 | 0.827 | 0.080 | 11 | 5807854 | intron variant | G/C;T | snv | 7 | |||
rs6547741 | 0.807 | 0.080 | 2 | 27633057 | intron variant | G/A | snv | 0.53 | 7 | ||
rs77452476 | 0.827 | 0.080 | 9 | 131087186 | intron variant | T/G | snv | 0.18 | 7 | ||
rs79767424 | 0.827 | 0.080 | 5 | 19108581 | intron variant | G/T | snv | 4.1E-02 | 7 | ||
rs8181047 | 0.807 | 0.120 | 9 | 22064466 | intron variant | A/G | snv | 0.79 | 7 | ||
rs10462706 | 0.827 | 0.080 | 5 | 1343679 | intron variant | C/T | snv | 0.14 | 6 | ||
rs10851478 | 0.827 | 0.080 | 15 | 49536822 | intron variant | T/C | snv | 0.30 | 6 | ||
rs1800628 | 0.827 | 0.080 | 6 | 31579073 | downstream gene variant | G/A | snv | 7.3E-02 | 6 | ||
rs2398180 | 0.827 | 0.080 | 15 | 96319940 | intron variant | C/T | snv | 0.62 | 6 | ||
rs3129780 | 0.827 | 0.080 | 6 | 32679924 | intergenic variant | T/A;C | snv | 6 | |||
rs928674 | 0.827 | 0.080 | 9 | 131076637 | intron variant | A/G | snv | 0.16 | 6 |