Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2299939 | 0.827 | 0.080 | 10 | 87897393 | intron variant | C/A;T | snv | 5 | |||
rs12334811 | 0.851 | 0.080 | 8 | 47920417 | intron variant | G/A | snv | 0.15 | 4 | ||
rs75790006 | 0.851 | 0.040 | 4 | 43211547 | intron variant | T/G | snv | 1.1E-02 | 4 | ||
rs8178085 | 0.851 | 0.080 | 8 | 47898144 | intron variant | T/G | snv | 2.3E-02 | 4 | ||
rs12934561 | 0.882 | 0.080 | 16 | 3068864 | intron variant | T/C | snv | 0.57 | 3 | ||
rs1340420 | 0.925 | 0.080 | 10 | 91857549 | intron variant | A/G | snv | 0.71 | 0.70 | 3 | |
rs1770474 | 0.925 | 0.080 | 10 | 91833770 | intron variant | G/A;T | snv | 3 | |||
rs181696 | 0.925 | 0.080 | 3 | 155548315 | intron variant | T/C | snv | 0.55 | 3 | ||
rs2847281 | 1.000 | 0.040 | 18 | 12821594 | intron variant | A/G | snv | 0.32 | 3 | ||
rs4268748 | 0.925 | 0.080 | 16 | 89960104 | intron variant | T/C | snv | 0.30 | 3 | ||
rs471692 | 0.925 | 0.080 | 17 | 40400518 | intron variant | T/A;C | snv | 0.79 | 3 | ||
rs4822983 | 0.925 | 0.080 | 22 | 28719078 | intron variant | C/T | snv | 0.33 | 3 | ||
rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
rs17761864 | 1.000 | 0.040 | 17 | 2268343 | intron variant | C/A | snv | 0.28 | 2 | ||
rs2239612 | 1.000 | 0.040 | 3 | 187075454 | intron variant | G/A | snv | 0.17 | 2 | ||
rs4785204 | 1.000 | 0.040 | 16 | 50069823 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs6819385 | 0.925 | 0.080 | 4 | 40337557 | intron variant | A/G | snv | 0.52 | 2 | ||
rs7182283 | 0.925 | 0.120 | 15 | 75351418 | intron variant | G/T | snv | 0.43 | 2 | ||
rs754626 | 0.925 | 0.080 | 20 | 37388937 | intron variant | T/G | snv | 0.25 | 2 | ||
rs1078305 | 1.000 | 0.040 | 9 | 121289122 | intron variant | A/G | snv | 0.70 | 1 | ||
rs10818524 | 1.000 | 0.040 | 9 | 121267901 | intron variant | T/C | snv | 0.37 | 1 | ||
rs11707807 | 1.000 | 0.040 | 3 | 188370473 | intron variant | A/G | snv | 0.36 | 1 | ||
rs117984432 | 1.000 | 0.040 | 16 | 89388583 | intron variant | T/C | snv | 2.0E-02 | 1 | ||
rs13301660 | 1.000 | 0.040 | 9 | 136446350 | intron variant | C/T | snv | 0.20 | 1 | ||
rs1460816 | 1.000 | 0.040 | 13 | 32354271 | intron variant | G/A | snv | 0.54 | 1 |