Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1994321 | 1.000 | 0.040 | 11 | 12065766 | upstream gene variant | G/T | snv | 0.33 | 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 | ||
rs34102224 | 0.925 | 0.040 | 8 | 5364506 | downstream gene variant | G/C | snv | 0.12 | 3 | ||
rs34467936 | 1.000 | 0.040 | 11 | 47893747 | intergenic variant | A/G | snv | 0.30 | 3 | ||
rs3843954 | 1.000 | 0.040 | 13 | 57974377 | intergenic variant | G/A;C | snv | 3 | |||
rs56388524 | 0.925 | 0.040 | 5 | 45757459 | intergenic variant | C/A;T | snv | 2.0E-02 | 3 | ||
rs61572747 | 1.000 | 0.040 | 17 | 45383525 | regulatory region variant | A/G | snv | 0.25 | 3 | ||
rs6546604 | 0.925 | 0.040 | 2 | 70415675 | intron variant | G/A;T | snv | 3 | |||
rs73720034 | 1.000 | 0.040 | 7 | 125794995 | intergenic variant | T/C | snv | 7.2E-02 | 3 | ||
rs74860738 | 0.925 | 0.040 | 11 | 80671683 | intergenic variant | G/A | snv | 7.2E-02 | 3 | ||
rs75995702 | 0.925 | 0.040 | 11 | 42785177 | intergenic variant | C/G;T | snv | 3 | |||
rs7613360 | 1.000 | 0.040 | 3 | 49879277 | upstream gene variant | C/T | snv | 0.32 | 3 | ||
rs78087832 | 0.925 | 0.040 | 2 | 224600060 | intergenic variant | C/T | snv | 2.4E-03 | 3 | ||
rs7939345 | 1.000 | 0.040 | 11 | 47959016 | intergenic variant | T/A;G | snv | 3 | |||
rs8100891 | 1.000 | 0.040 | 19 | 32338607 | intergenic variant | C/A;G | snv | 3 | |||
rs143405544 | 0.925 | 0.040 | 5 | 65459777 | intron variant | A/G | snv | 4.8E-03 | 3 | ||
rs1789891 | 1.000 | 0.080 | 4 | 99329262 | intron variant | C/A | snv | 0.13 | 3 | ||
rs35825582 | 1.000 | 0.040 | 2 | 143491193 | intron variant | G/A | snv | 0.45 | 3 | ||
rs188843168 | 0.925 | 0.040 | 10 | 103390184 | intron variant | T/A;C | snv | 4.3E-04 | 3 | ||
rs77945277 | 0.925 | 0.040 | 14 | 34840969 | intron variant | A/G | snv | 4.9E-03 | 3 | ||
rs138472420 | 1.000 | 0.040 | 19 | 47657765 | intron variant | G/A | snv | 3.3E-03 | 3 | ||
rs6063349 | 0.925 | 0.040 | 20 | 49065345 | intron variant | G/A;C;T | snv | 3 | |||
rs142641502 | 0.925 | 0.040 | 11 | 33109861 | intron variant | T/C | snv | 8.0E-03 | 3 | ||
rs4839421 | 0.925 | 0.040 | 1 | 110479338 | intron variant | C/A | snv | 0.40 | 3 |