Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4958881 | 0.827 | 0.280 | 5 | 151070675 | intron variant | T/C | snv | 0.21 | 1 | ||
rs1020388 | 5 | 56264200 | upstream gene variant | T/G | snv | 0.34 | 2 | ||||
rs10932019 | 2 | 203764087 | downstream gene variant | G/A;C | snv | 2 | |||||
rs1355208 | 2 | 30222456 | intergenic variant | A/G | snv | 0.65 | 2 | ||||
rs2155433 | 11 | 118742212 | intron variant | G/A | snv | 0.24 | 2 | ||||
rs4626515 | 7 | 140204330 | intergenic variant | T/C | snv | 0.22 | 2 | ||||
rs636393 | 6 | 137686393 | intron variant | G/T | snv | 0.66 | 2 | ||||
rs6848139 | 1.000 | 0.040 | 4 | 122473886 | intergenic variant | A/C;G | snv | 2 | |||
rs6933404 | 0.925 | 0.280 | 6 | 137638098 | intergenic variant | T/C | snv | 0.16 | 2 | ||
rs7579944 | 0.882 | 0.200 | 2 | 30222160 | intergenic variant | T/C;G | snv | 2 | |||
rs906868 | 0.925 | 0.120 | 2 | 30225478 | intergenic variant | G/T | snv | 0.53 | 2 | ||
rs975730 | 8 | 128303768 | intergenic variant | G/A | snv | 0.45 | 2 | ||||
rs10892286 | 11 | 118771376 | intron variant | A/C | snv | 0.17 | 2 | ||||
rs11984075 | 7 | 37397251 | intron variant | A/G | snv | 0.14 | 2 | ||||
rs1772408 | 1 | 159035859 | intron variant | A/G;T | snv | 2 | |||||
rs2893008 | 4 | 122631659 | intron variant | A/G | snv | 5.1E-02 | 2 | ||||
rs4288027 | 4 | 122262050 | intron variant | A/C;G | snv | 0.13 | 2 | ||||
rs4374642 | 4 | 122179956 | intron variant | T/C | snv | 0.13 | 2 | ||||
rs7678445 | 4 | 122361617 | intron variant | G/A;T | snv | 2 | |||||
rs10460003 | 18 | 12747013 | intron variant | C/T | snv | 0.15 | 2 | ||||
rs11043097 | 11 | 11114248 | intron variant | T/C | snv | 0.15 | 2 | ||||
rs7523907 | 1.000 | 0.080 | 1 | 167458010 | non coding transcript exon variant | C/A;T | snv | 2 | |||
rs9295089 | 6 | 159042932 | non coding transcript exon variant | T/C | snv | 0.20 | 2 | ||||
rs10752747 | 1 | 2593476 | intron variant | G/T | snv | 0.41 | 2 | ||||
rs12138909 | 1 | 2607299 | intron variant | C/T | snv | 0.11 | 2 |