Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10024899 | 4 | 121705035 | intergenic variant | T/C | snv | 0.35 | 1 | ||||
rs10070064 | 5 | 173854774 | intergenic variant | C/T | snv | 0.26 | 1 | ||||
rs10458575 | 1 | 65104082 | regulatory region variant | T/C | snv | 0.45 | 1 | ||||
rs10464079 | 5 | 179098778 | intergenic variant | G/A | snv | 0.71 | 1 | ||||
rs10475249 | 5 | 4010021 | downstream gene variant | C/G | snv | 0.45 | 1 | ||||
rs10490869 | 3 | 35593653 | intergenic variant | A/T | snv | 0.15 | 1 | ||||
rs10501039 | 11 | 26152856 | intergenic variant | T/C | snv | 4.5E-02 | 1 | ||||
rs10507223 | 12 | 108062051 | intergenic variant | C/G | snv | 0.17 | 1 | ||||
rs10763957 | 10 | 33877770 | regulatory region variant | C/T | snv | 0.35 | 1 | ||||
rs10827252 | 10 | 33383956 | upstream gene variant | A/G | snv | 0.51 | 1 | ||||
rs10844642 | 12 | 33577433 | downstream gene variant | A/C | snv | 0.27 | 1 | ||||
rs10851523 | 15 | 52751805 | downstream gene variant | G/A;C | snv | 1 | |||||
rs10880321 | 12 | 37976308 | intergenic variant | C/A;G | snv | 1 | |||||
rs10991433 | 9 | 104964637 | intergenic variant | T/C | snv | 8.2E-02 | 1 | ||||
rs10992408 | 9 | 92682518 | intergenic variant | A/G | snv | 0.20 | 1 | ||||
rs10993017 | 9 | 93998102 | intergenic variant | T/A;C | snv | 0.31 | 1 | ||||
rs11055887 | 12 | 14264245 | intergenic variant | G/A | snv | 0.14 | 1 | ||||
rs11059476 | 12 | 122708052 | intron variant | C/T | snv | 3.9E-02 | 1 | ||||
rs11176015 | 12 | 66047904 | intergenic variant | C/T | snv | 0.32 | 1 | ||||
rs11187140 | 10 | 92707153 | downstream gene variant | G/A | snv | 0.29 | 1 | ||||
rs11187742 | 10 | 93966124 | upstream gene variant | A/G;T | snv | 1 | |||||
rs11202585 | 10 | 87849022 | downstream gene variant | G/C | snv | 0.18 | 1 | ||||
rs1122080 | 5 | 158588895 | downstream gene variant | G/A | snv | 0.21 | 1 | ||||
rs1122157 | 10 | 62101841 | downstream gene variant | C/A;T | snv | 1 | |||||
rs112266013 | 6 | 15230512 | intergenic variant | G/A | snv | 0.12 | 1 |