Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 25 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 23 | ||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 16 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 16 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 14 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 12 | |||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 11 | ||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 11 | |||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 9 | ||
rs1800437 | 0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 | 9 | |
rs2112347 | 0.925 | 0.120 | 5 | 75719417 | upstream gene variant | T/G | snv | 0.42 | 9 | ||
rs7498665 | 0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 | 8 | ||
rs987237 | 0.925 | 0.120 | 6 | 50835337 | intron variant | A/G | snv | 0.17 | 8 | ||
rs9930506 | 0.776 | 0.360 | 16 | 53796553 | intron variant | A/G | snv | 0.36 | 8 | ||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 8 | ||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 7 | ||
rs10968576 | 0.882 | 0.120 | 9 | 28414341 | intron variant | A/G | snv | 0.26 | 7 | ||
rs12149832 | 0.851 | 0.120 | 16 | 53808996 | intron variant | G/A | snv | 0.31 | 7 | ||
rs12446632 | 1.000 | 0.080 | 16 | 19924067 | intergenic variant | G/A | snv | 0.11 | 7 | ||
rs13130484 | 1.000 | 0.080 | 4 | 45173674 | intergenic variant | C/A;T | snv | 7 | |||
rs1516725 | 0.925 | 0.120 | 3 | 186106215 | intron variant | T/C | snv | 0.86 | 7 | ||
rs17817449 | 0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv | 7 | |||
rs2531995 | 1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 | 7 | ||
rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 7 | |||
rs3751812 | 0.882 | 0.160 | 16 | 53784548 | intron variant | G/T | snv | 0.30 | 7 |