Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs238415 | 0.851 | 0.120 | 19 | 45353977 | intron variant | C/A;G;T | snv | 4 | |||
rs3916874 | 0.851 | 0.120 | 19 | 45353668 | intron variant | C/A;G | snv | 0.19 | 4 | ||
rs107822 | 0.827 | 0.120 | 6 | 33207798 | upstream gene variant | C/T | snv | 0.27 | 0.28 | 5 | |
rs451360 | 0.827 | 0.200 | 5 | 1319565 | intron variant | C/A;T | snv | 5 | |||
rs2736108 | 0.807 | 0.160 | 5 | 1297373 | upstream gene variant | C/T | snv | 0.24 | 6 | ||
rs664677 | 0.807 | 0.160 | 11 | 108272455 | intron variant | C/A;T | snv | 0.65 | 8 | ||
rs2072454 | 0.763 | 0.160 | 7 | 55146655 | synonymous variant | C/T | snv | 0.51 | 0.51 | 9 | |
rs3764340 | 0.807 | 0.280 | 16 | 78432540 | missense variant | C/G | snv | 7.1E-02 | 7.4E-02 | 9 | |
rs140693 | 0.763 | 0.280 | 3 | 129436608 | missense variant | C/T | snv | 5.8E-02 | 3.1E-02 | 10 | |
rs3731239 | 0.763 | 0.240 | 9 | 21974219 | intron variant | A/G | snv | 0.26 | 10 | ||
rs10511729 | 0.742 | 0.240 | 9 | 23557229 | intron variant | T/G | snv | 0.35 | 11 | ||
rs10811474 | 0.742 | 0.240 | 9 | 21114238 | intergenic variant | A/G | snv | 0.44 | 11 | ||
rs12683422 | 0.742 | 0.240 | 9 | 27969442 | intron variant | C/T | snv | 5.7E-02 | 11 | ||
rs213210 | 0.742 | 0.240 | 6 | 33208047 | upstream gene variant | A/C;G | snv | 11 | |||
rs2073498 | 0.763 | 0.280 | 3 | 50332115 | missense variant | C/A | snv | 9.6E-02 | 8.0E-02 | 12 | |
rs13042395 | 0.752 | 0.160 | 20 | 773867 | intron variant | C/T | snv | 5.9E-02 | 13 | ||
rs3213245 | 0.742 | 0.240 | 19 | 43575535 | 5 prime UTR variant | G/A | snv | 0.65 | 0.60 | 13 | |
rs3813867 | 0.732 | 0.240 | 10 | 133526101 | intron variant | G/A;C | snv | 13 | |||
rs667282 | 0.790 | 0.120 | 15 | 78571130 | intron variant | T/C | snv | 0.28 | 13 | ||
rs2151280 | 0.701 | 0.360 | 9 | 22034720 | non coding transcript exon variant | G/A | snv | 0.46 | 16 | ||
rs7003908 | 0.716 | 0.320 | 8 | 47858141 | intron variant | C/A | snv | 0.66 | 16 | ||
rs121913444 | 0.724 | 0.160 | 7 | 55191831 | missense variant | T/A;C;G | snv | 18 | |||
rs1805377 | 0.689 | 0.480 | 5 | 83353124 | splice acceptor variant | G/A | snv | 0.23 | 0.25 | 19 | |
rs2267437 | 0.724 | 0.320 | 22 | 41620695 | intron variant | C/A;G | snv | 19 | |||
rs937283 | 0.716 | 0.200 | 12 | 68808384 | 5 prime UTR variant | A/G | snv | 0.37 | 19 |