Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs62117160 | 0.925 | 0.120 | 19 | 44728895 | upstream gene variant | G/A;T | snv | 3 | |||
rs712484 | 0.882 | 0.160 | 14 | 48081576 | intergenic variant | C/A | snv | 0.14 | 3 | ||
rs7124842 | 0.882 | 0.160 | 11 | 76600576 | intergenic variant | G/A;C;T | snv | 3 | |||
rs7713145 | 1.000 | 0.040 | 5 | 177354208 | upstream gene variant | G/A | snv | 0.37 | 3 | ||
rs878860 | 0.882 | 0.120 | 11 | 7946812 | intergenic variant | C/T | snv | 0.35 | 3 | ||
rs112111458 | 0.925 | 0.120 | 2 | 70872975 | intergenic variant | A/G | snv | 0.16 | 2 | ||
rs11242709 | 1.000 | 0.040 | 6 | 209159 | upstream gene variant | C/T | snv | 0.19 | 2 | ||
rs11255753 | 1.000 | 0.040 | 10 | 8563590 | intergenic variant | G/C;T | snv | 0.23 | 2 | ||
rs2164983 | 0.925 | 0.120 | 19 | 8679120 | downstream gene variant | C/A;G | snv | 0.19 | 2 | ||
rs224108 | 0.925 | 0.120 | 10 | 62789851 | intron variant | T/C;G | snv | 0.21 | 2 | ||
rs2744939 | 1.000 | 0.040 | 6 | 34580429 | upstream gene variant | T/A | snv | 0.17 | 2 | ||
rs4939490 | 0.925 | 0.120 | 11 | 61026179 | intergenic variant | C/G | snv | 0.39 | 2 | ||
rs519973 | 1.000 | 0.040 | 3 | 187915480 | intergenic variant | G/A | snv | 0.33 | 2 | ||
rs5743399 | 0.925 | 0.120 | 8 | 6880123 | intron variant | G/A | snv | 0.31 | 2 | ||
rs61192126 | 1.000 | 0.040 | 3 | 72345701 | intergenic variant | T/C | snv | 0.26 | 2 | ||
rs6473227 | 0.925 | 0.120 | 8 | 80373657 | intron variant | C/A | snv | 0.54 | 2 | ||
rs76167968 | 1.000 | 0.040 | 1 | 35216137 | intergenic variant | T/C | snv | 0.25 | 2 | ||
rs10131567 | 1.000 | 0.040 | 14 | 35395672 | intergenic variant | G/T | snv | 0.22 | 1 | ||
rs10244416 | 1.000 | 0.040 | 7 | 20536128 | intergenic variant | C/A;T | snv | 0.52 | 1 | ||
rs10468514 | 1.000 | 0.040 | 17 | 45378874 | intergenic variant | A/G | snv | 0.38 | 1 | ||
rs10489854 | 1.000 | 0.040 | 1 | 159279069 | non coding transcript exon variant | C/T | snv | 8.3E-02 | 1 | ||
rs111267073 | 1.000 | 0.040 | 5 | 111030094 | intergenic variant | C/T | snv | 1.9E-02 | 1 | ||
rs11213941 | 1.000 | 0.040 | 11 | 111563369 | downstream gene variant | T/C | snv | 0.35 | 1 | ||
rs114997373 | 1.000 | 0.040 | 1 | 45535906 | downstream gene variant | G/A | snv | 1.2E-02 | 1 | ||
rs118013485 | 1.000 | 0.040 | 19 | 33235671 | TF binding site variant | G/A | snv | 5.0E-02 | 1 |