Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1415259 | 0.925 | 0.080 | 1 | 162115519 | intron variant | C/T | snv | 0.54 | 2 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 2 | ||
rs9825823 | 0.851 | 0.080 | 3 | 61096480 | intron variant | T/C | snv | 0.47 | 2 | ||
rs1082214 | 0.925 | 0.080 | 12 | 56452706 | non coding transcript exon variant | C/T | snv | 9.3E-02 | 1 | ||
rs1106634 | 0.851 | 0.080 | 8 | 20208538 | intron variant | G/A;C;T | snv | 0.18 | 1 | ||
rs11824092 | 0.925 | 0.080 | 11 | 13324747 | intron variant | T/C | snv | 0.62 | 1 | ||
rs120074175 | 0.827 | 0.080 | 12 | 72031544 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs139315125 | 0.851 | 0.080 | 1 | 7809900 | missense variant | A/G | snv | 5.6E-03 | 5.0E-03 | 1 | |
rs1488864 | 0.851 | 0.080 | 11 | 6321099 | intron variant | T/G | snv | 0.80 | 1 | ||
rs1491850 | 0.925 | 0.080 | 11 | 27728178 | intron variant | T/C | snv | 0.37 | 1 | ||
rs2522833 | 0.827 | 0.080 | 7 | 82824392 | missense variant | A/C | snv | 0.45 | 0.34 | 1 | |
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs33939927 | 0.708 | 0.120 | 12 | 40310434 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
rs4523957 | 0.790 | 0.120 | 17 | 2305605 | intron variant | G/T | snv | 0.54 | 2 | ||
rs528732638 | 0.851 | 0.120 | 18 | 26940224 | intron variant | A/-;AA;AAA;AAAA | delins | 2 | |||
rs10514299 | 0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 | 1 | ||
rs11754661 | 0.851 | 0.120 | 6 | 150885942 | intron variant | G/A;T | snv | 1 | |||
rs12912233 | 0.851 | 0.120 | 15 | 60974897 | intron variant | C/T | snv | 0.38 | 1 | ||
rs1545843 | 0.827 | 0.120 | 12 | 84170289 | intron variant | G/A | snv | 0.52 | 1 | ||
rs2028122 | 0.851 | 0.120 | 15 | 60549076 | intron variant | A/G | snv | 0.51 | 1 | ||
rs2300478 | 0.851 | 0.120 | 2 | 66554321 | intron variant | T/G | snv | 0.21 | 1 | ||
rs34436714 | 0.851 | 0.120 | 19 | 53824059 | missense variant | C/A;T | snv | 0.22 | 1 | ||
rs1131691771 | 0.807 | 0.160 | 6 | 78958469 | splice donor variant | ACTT/- | delins | 18 | |||
rs7103411 | 0.752 | 0.160 | 11 | 27678578 | intron variant | C/T | snv | 0.82 | 3 | ||
rs1863918 | 0.882 | 0.160 | 5 | 179112381 | 3 prime UTR variant | G/T | snv | 0.25 | 1 |