Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 16 | |||
rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 12 | ||
rs10810657 | 0.827 | 0.080 | 9 | 16884588 | regulatory region variant | T/A;G | snv | 7 | |||
rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 7 | ||
rs1246946 | 0.851 | 0.040 | 6 | 4979722 | downstream gene variant | C/T | snv | 0.34 | 4 | ||
rs4761496 | 0.851 | 0.040 | 12 | 94733833 | regulatory region variant | T/A;C | snv | 0.23 | 4 | ||
rs75790006 | 0.851 | 0.040 | 4 | 43211547 | intron variant | T/G | snv | 1.1E-02 | 4 | ||
rs12296850 | 0.925 | 0.080 | 12 | 100426307 | downstream gene variant | A/G | snv | 8.7E-02 | 3 | ||
rs7309332 | 1.000 | 0.040 | 12 | 7938243 | upstream gene variant | T/C | snv | 0.59 | 3 | ||
rs74664507 | 1.000 | 0.040 | 9 | 16913838 | upstream gene variant | T/A | snv | 3 | |||
rs1412115 | 0.925 | 0.080 | 10 | 33799125 | regulatory region variant | T/C | snv | 0.58 | 2 | ||
rs6503659 | 1.000 | 0.040 | 17 | 41741012 | intergenic variant | A/C;G;T | snv | 2 | |||
rs35324266 | 1.000 | 0.040 | 6 | 32625467 | upstream gene variant | C/T | snv | 0.16 | 1 | ||
rs62209647 | 1.000 | 0.040 | 20 | 33917852 | upstream gene variant | G/C | snv | 4.4E-02 | 1 | ||
rs6791479 | 1.000 | 0.040 | 3 | 189487243 | intergenic variant | T/A | snv | 0.48 | 1 | ||
rs7097008 | 1.000 | 0.040 | 10 | 67849782 | non coding transcript exon variant | C/A | snv | 0.60 | 1 | ||
rs9557210 | 1.000 | 0.040 | 13 | 99395250 | intergenic variant | G/A | snv | 0.16 | 1 | ||
rs9651495 | 1.000 | 0.040 | 10 | 89172624 | regulatory region variant | G/A | snv | 0.13 | 1 | ||
rs774121564 | 1.000 | 0.040 | 2 | 275197 | missense variant | C/G | snv | 4.1E-06 | 1 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs1800625 | 0.641 | 0.680 | 6 | 32184665 | upstream gene variant | A/G | snv | 0.15 | 39 | ||
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs117984432 | 1.000 | 0.040 | 16 | 89388583 | intron variant | T/C | snv | 2.0E-02 | 1 | ||
rs1801166 | 0.732 | 0.200 | 5 | 112839543 | missense variant | G/C | snv | 4.4E-03 | 5.6E-03 | 17 |