Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4821112 | 22 | 21610472 | intron variant | G/A | snv | 0.21 | 4 | ||||
rs760361706 | 22 | 46235326 | missense variant | G/C | snv | 4.0E-06 | 4 | ||||
rs6498142 | 16 | 10987392 | intron variant | C/G | snv | 0.77 | 3 | ||||
rs926657 | 6 | 159042420 | non coding transcript exon variant | C/G;T | snv | 3 | |||||
rs1020388 | 5 | 56264200 | upstream gene variant | T/G | snv | 0.34 | 2 | ||||
rs10460003 | 18 | 12747013 | intron variant | C/T | snv | 0.15 | 2 | ||||
rs10752747 | 1 | 2593476 | intron variant | G/T | snv | 0.41 | 2 | ||||
rs10892286 | 11 | 118771376 | intron variant | A/C | snv | 0.17 | 2 | ||||
rs10932019 | 2 | 203764087 | downstream gene variant | G/A;C | snv | 2 | |||||
rs11043097 | 11 | 11114248 | intron variant | T/C | snv | 0.15 | 2 | ||||
rs1194849 | 2 | 65379519 | intron variant | T/C | snv | 0.49 | 2 | ||||
rs11984075 | 7 | 37397251 | intron variant | A/G | snv | 0.14 | 2 | ||||
rs12138909 | 1 | 2607299 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs1355208 | 2 | 30222456 | intergenic variant | A/G | snv | 0.65 | 2 | ||||
rs1772408 | 1 | 159035859 | intron variant | A/G;T | snv | 2 | |||||
rs1876518 | 2 | 65381775 | intron variant | C/T | snv | 0.45 | 2 | ||||
rs2155433 | 11 | 118742212 | intron variant | G/A | snv | 0.24 | 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 | ||||
rs4626515 | 7 | 140204330 | intergenic variant | T/C | snv | 0.22 | 2 | ||||
rs636393 | 6 | 137686393 | intron variant | G/T | snv | 0.66 | 2 | ||||
rs6706689 | 2 | 60943910 | intron variant | A/G | snv | 0.48 | 2 | ||||
rs7678445 | 4 | 122361617 | intron variant | G/A;T | snv | 2 | |||||
rs9295089 | 6 | 159042932 | non coding transcript exon variant | T/C | snv | 0.20 | 2 |