Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
rs2430561 | 0.590 | 0.760 | 12 | 68158742 | intron variant | T/A | snv | 0.36 | 50 | ||
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs153109 | 0.623 | 0.600 | 16 | 28507775 | intron variant | T/C | snv | 0.43 | 37 | ||
rs57095329 | 0.677 | 0.480 | 5 | 160467840 | intron variant | A/G | snv | 7.8E-02 | 25 | ||
rs10821936 | 0.742 | 0.200 | 10 | 61963818 | intron variant | C/T | snv | 0.69 | 11 | ||
rs3824662 | 0.752 | 0.320 | 10 | 8062245 | intron variant | C/A;T | snv | 11 | |||
rs3731217 | 0.763 | 0.320 | 9 | 21984662 | intron variant | A/C;T | snv | 10 | |||
rs7089424 | 0.752 | 0.200 | 10 | 61992400 | intron variant | T/G | snv | 0.32 | 10 | ||
rs11978267 | 0.763 | 0.240 | 7 | 50398606 | intron variant | A/G | snv | 0.25 | 9 | ||
rs2069727 | 0.763 | 0.320 | 12 | 68154443 | intron variant | T/A;C | snv | 9 | |||
rs1966862 | 0.790 | 0.120 | 4 | 85766908 | intron variant | A/G | snv | 0.14 | 8 | ||
rs10740055 | 0.790 | 0.240 | 10 | 61958720 | intron variant | C/A | snv | 0.49 | 7 | ||
rs10994982 | 0.790 | 0.120 | 10 | 61950345 | intron variant | A/G | snv | 0.49 | 7 | ||
rs924607 | 0.851 | 0.120 | 5 | 609978 | intron variant | C/T | snv | 0.32 | 7 | ||
rs210143 | 0.827 | 0.160 | 6 | 33579153 | intron variant | T/C | snv | 0.74 | 6 | ||
rs2413739 | 0.827 | 0.120 | 22 | 43001030 | intron variant | C/T | snv | 0.43 | 6 | ||
rs2036914 | 0.882 | 0.160 | 4 | 186271327 | intron variant | T/C | snv | 0.57 | 5 | ||
rs6021191 | 0.851 | 0.120 | 20 | 51419700 | intron variant | A/T | snv | 4.9E-02 | 5 | ||
rs6479778 | 0.827 | 0.200 | 10 | 61929318 | intron variant | T/C;G | snv | 5 | |||
rs1544105 | 0.851 | 0.200 | 9 | 127800446 | intron variant | C/T | snv | 0.48 | 4 | ||
rs17069665 | 0.882 | 0.120 | 6 | 108620265 | intron variant | A/C;G | snv | 4 | |||
rs6535455 | 0.851 | 0.160 | 4 | 83310951 | intron variant | T/A;C | snv | 4 | |||
rs7088318 | 0.851 | 0.120 | 10 | 22564019 | intron variant | C/A | snv | 0.55 | 4 | ||
rs10235796 | 0.882 | 0.120 | 7 | 50394939 | intron variant | T/C | snv | 0.82 | 3 |