Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 12 | ||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 7 | |
rs4650608 | 0.851 | 0.040 | 1 | 78772330 | intergenic variant | T/C | snv | 0.29 | 7 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
rs2252865 | 0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 | 6 | ||
rs1625579 | 0.763 | 0.160 | 1 | 98037378 | intron variant | G/T | snv | 0.78 | 5 | ||
rs4130548 | 1.000 | 0.040 | 1 | 77998184 | intron variant | T/C | snv | 0.25 | 5 | ||
rs6694545 | 0.851 | 0.040 | 1 | 29964421 | intergenic variant | A/G | snv | 0.58 | 5 | ||
rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 4 | ||
rs6586354 | 0.851 | 0.040 | 1 | 234897489 | intron variant | G/A | snv | 0.25 | 4 | ||
rs11210892 | 1.000 | 0.040 | 1 | 43634413 | intergenic variant | G/A | snv | 0.51 | 3 | ||
rs115777110 | 0.882 | 0.040 | 1 | 208936211 | intergenic variant | T/C | snv | 1.2E-02 | 3 | ||
rs12061601 | 1.000 | 0.040 | 1 | 169101212 | intron variant | T/C | snv | 0.16 | 3 | ||
rs12128108 | 0.925 | 0.040 | 1 | 49827749 | intron variant | C/G;T | snv | 3 | |||
rs12561919 | 1.000 | 0.040 | 1 | 11779866 | missense variant | C/T | snv | 0.13 | 0.13 | 3 | |
rs146330533 | 0.882 | 0.040 | 1 | 17669971 | intron variant | G/A | snv | 1.2E-02 | 3 | ||
rs3027001 | 1.000 | 0.040 | 1 | 159199673 | intron variant | C/G;T | snv | 3 | |||
rs3747631 | 1.000 | 0.040 | 1 | 204618441 | missense variant | G/A;C | snv | 4.0E-06; 0.20 | 3 | ||
rs4949526 | 1.000 | 0.040 | 1 | 29959372 | intergenic variant | T/C | snv | 0.54 | 3 | ||
rs6703335 | 0.882 | 0.040 | 1 | 243445665 | intron variant | A/G | snv | 0.50 | 3 | ||
rs1008078 | 1.000 | 0.040 | 1 | 90724174 | non coding transcript exon variant | C/T | snv | 0.33 | 2 | ||
rs10489202 | 0.925 | 0.080 | 1 | 167933841 | intron variant | G/T | snv | 0.20 | 2 | ||
rs11209970 | 1.000 | 0.040 | 1 | 41377768 | intron variant | G/A | snv | 0.59 | 2 | ||
rs11210195 | 1.000 | 0.040 | 1 | 73283600 | intergenic variant | C/T | snv | 0.44 | 2 | ||
rs12124523 | 1.000 | 0.040 | 1 | 72155780 | intron variant | C/T | snv | 7.0E-02 | 2 |