Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1081432 | 1.000 | 0.080 | 2 | 6708412 | intergenic variant | T/C | snv | 1 | |||
rs1229544 | 1.000 | 0.080 | 7 | 97793192 | intergenic variant | C/T | snv | 4.6E-02 | 1 | ||
rs12309362 | 1.000 | 0.080 | 12 | 132466447 | downstream gene variant | G/A;T | snv | 1 | |||
rs1502174 | 1.000 | 0.080 | 3 | 135550249 | intergenic variant | A/G | snv | 0.46 | 1 | ||
rs2064836 | 1.000 | 0.080 | X | 92628018 | downstream gene variant | A/G;T | snv | 1 | |||
rs2198843 | 1.000 | 0.080 | 15 | 74708889 | regulatory region variant | C/G;T | snv | 1 | |||
rs2275959 | 1.000 | 0.080 | 8 | 37597541 | non coding transcript exon variant | G/A;C | snv | 1 | |||
rs3997872 | 1.000 | 0.080 | 6 | 32612840 | intergenic variant | T/A | snv | 0.14 | 1 | ||
rs405 | 1.000 | 0.080 | 7 | 91917013 | intergenic variant | G/A;C;T | snv | 1 | |||
rs584368 | 1.000 | 0.080 | 11 | 88232053 | regulatory region variant | C/T | snv | 0.70 | 1 | ||
rs6025211 | 1.000 | 0.080 | 20 | 56864307 | intergenic variant | C/G;T | snv | 1 | |||
rs6078460 | 1.000 | 0.080 | 20 | 12116249 | intergenic variant | A/C;G;T | snv | 1 | |||
rs649053 | 1.000 | 0.080 | 9 | 21387419 | upstream gene variant | A/G;T | snv | 1 | |||
rs7821974 | 1.000 | 0.080 | 8 | 37592483 | downstream gene variant | T/C | snv | 0.22 | 1 | ||
rs8113007 | 1.000 | 0.080 | 19 | 39252463 | upstream gene variant | A/T | snv | 0.29 | 1 | ||
rs878461 | 1.000 | 0.080 | 2 | 127415841 | upstream gene variant | T/C;G | snv | 0.11 | 1 | ||
rs9877457 | 1.000 | 0.080 | 3 | 135564539 | intergenic variant | A/G;T | snv | 1 | |||
rs9970827 | 1.000 | 0.080 | 1 | 185409746 | regulatory region variant | G/A | snv | 0.37 | 1 | ||
rs201159898 | 1.000 | 0.080 | 7 | 87549509 | missense variant | T/A;C | snv | 1.2E-05 | 4.9E-05 | 1 | |
rs28364274 | 1.000 | 0.080 | 7 | 87504335 | missense variant | C/T | snv | 4.7E-03 | 4.6E-03 | 1 | |
rs45456698 | 1.000 | 0.080 | 7 | 87504335 | missense variant | C/T | snv | 1 | |||
rs762334560 | 1.000 | 0.080 | 4 | 73404391 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs397514032 | 1.000 | 0.080 | 5 | 112828923 | frameshift variant | A/- | delins | 1 | |||
rs2267401 | 1.000 | 0.080 | 22 | 38982116 | intron variant | T/A;G | snv | 1 | |||
rs760125354 | 1.000 | 0.080 | 22 | 38991371 | stop gained | G/C;T | snv | 1 |