Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12555870 | 0.925 | 0.040 | 9 | 23347726 | intron variant | A/G | snv | 0.36 | 3 | ||
rs1411216 | 0.925 | 0.040 | 9 | 24520196 | intergenic variant | A/G | snv | 0.73 | 3 | ||
rs142484554 | 0.925 | 0.040 | 3 | 141059454 | intron variant | GAG/- | delins | 0.11 | 3 | ||
rs142641502 | 0.925 | 0.040 | 11 | 33109861 | intron variant | T/C | snv | 8.0E-03 | 3 | ||
rs143405544 | 0.925 | 0.040 | 5 | 65459777 | intron variant | A/G | snv | 4.8E-03 | 3 | ||
rs143934587 | 0.925 | 0.040 | 20 | 19165806 | intergenic variant | G/A | snv | 9.1E-03 | 3 | ||
rs1548076 | 0.925 | 0.040 | 15 | 69934284 | intergenic variant | G/A | snv | 0.95 | 3 | ||
rs182377406 | 0.925 | 0.040 | 11 | 67449378 | upstream gene variant | A/G | snv | 4.5E-04 | 3 | ||
rs183042538 | 0.925 | 0.040 | 20 | 41197420 | intron variant | A/T | snv | 3.2E-02 | 3 | ||
rs183124483 | 0.925 | 0.040 | 17 | 28110028 | intron variant | G/A | snv | 7.1E-04 | 3 | ||
rs188843168 | 0.925 | 0.040 | 10 | 103390184 | intron variant | T/A;C | snv | 4.3E-04 | 3 | ||
rs189864513 | 0.925 | 0.040 | 4 | 52767390 | intron variant | T/C | snv | 1.9E-03 | 3 | ||
rs190783615 | 0.925 | 0.040 | X | 142772620 | intergenic variant | T/C | snv | 9.3E-03 | 3 | ||
rs1908557 | 0.925 | 0.040 | 4 | 89500202 | intron variant | T/C | snv | 0.31 | 3 | ||
rs200855945 | 0.925 | 0.040 | 12 | 26124961 | 5 prime UTR variant | ACACGCACAC/-;ACACGCACACACACGCACAC | delins | 1.6E-02 | 3 | ||
rs201203751 | 0.925 | 0.040 | 5 | 39203496 | intron variant | TT/-;T;TTT | delins | 3 | |||
rs201569130 | 0.925 | 0.040 | 6 | 1402916 | intergenic variant | GACA/- | delins | 1.1E-02 | 3 | ||
rs201921722 | 0.925 | 0.040 | 11 | 123679999 | downstream gene variant | -/A | delins | 9.2E-06 | 3 | ||
rs2979204 | 0.925 | 0.040 | 8 | 8441347 | regulatory region variant | T/C | snv | 0.34 | 3 | ||
rs34102224 | 0.925 | 0.040 | 8 | 5364506 | downstream gene variant | G/C | snv | 0.12 | 3 | ||
rs34177316 | 0.925 | 0.040 | 4 | 40985283 | intron variant | A/-;AA;AAA | delins | 3 | |||
rs352759 | 0.925 | 0.040 | 8 | 15742205 | intron variant | T/A | snv | 3 | |||
rs35792458 | 0.925 | 0.040 | 8 | 10964921 | intron variant | G/C | snv | 0.53 | 3 | ||
rs4761545 | 0.925 | 0.040 | 12 | 94032692 | regulatory region variant | G/T | snv | 0.56 | 3 | ||
rs4839421 | 0.925 | 0.040 | 1 | 110479338 | intron variant | C/A | snv | 0.40 | 3 |