Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1034207 | 6 | 127016554 | intron variant | C/A;G;T | snv | 0.94 | 1 | ||||
rs11154370 | 6 | 126846446 | intron variant | A/G;T | snv | 1 | |||||
rs1443512 | 12 | 53948900 | downstream gene variant | A/C;T | snv | 1 | |||||
rs17568628 | 5 | 76751114 | intergenic variant | T/C;G | snv | 1 | |||||
rs2119690 | 8 | 20002028 | intergenic variant | G/A;C | snv | 1 | |||||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 1 | |||||
rs4580892 | 6 | 127088737 | intron variant | C/T | snv | 0.32 | 1 | ||||
rs4846567 | 1 | 219577375 | regulatory region variant | G/T | snv | 0.23 | 1 | ||||
rs645040 | 3 | 136207780 | upstream gene variant | G/T | snv | 0.77 | 1 | ||||
rs757608 | 17 | 61419916 | regulatory region variant | A/G;T | snv | 1 | |||||
rs7797307 | 7 | 69221140 | intron variant | G/C | snv | 7.6E-02 | 1 | ||||
rs9750952 | 1.000 | 0.080 | 2 | 238827723 | intergenic variant | C/T | snv | 0.19 | 1 | ||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 1 | |||
rs1254319 | 1.000 | 14 | 60437039 | missense variant | G/A | snv | 0.35 | 0.36 | 1 | ||
rs459193 | 0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 | 1 | ||
rs505102 | 1 | 196650372 | upstream gene variant | T/C | snv | 0.40 | 1 | ||||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 1 | |||
rs9515201 | 0.925 | 0.080 | 13 | 110388451 | intron variant | A/C | snv | 0.63 | 1 | ||
rs6861681 | 5 | 173935455 | intron variant | G/A | snv | 0.22 | 1 | ||||
rs6942652 | 7 | 121249218 | intron variant | G/C;T | snv | 1 | |||||
rs11724804 | 0.882 | 0.160 | 4 | 971991 | intron variant | G/A | snv | 0.43 | 1 | ||
rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 1 | ||||
rs605203 | 1.000 | 0.120 | 6 | 31879235 | intron variant | C/A | snv | 0.77 | 1 | ||
rs9647379 | 3 | 172067378 | intron variant | G/C | snv | 0.32 | 1 | ||||
rs9302652 | 1.000 | 0.080 | 16 | 53832063 | intron variant | C/T | snv | 0.74 | 1 |