Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 13 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 9 | ||
rs7953257 | 12 | 112246417 | intron variant | A/G;T | snv | 0.71 | 5 | ||||
rs555346412 | 12 | 112191863 | intron variant | G/C | snv | 8.2E-04 | 5 | ||||
rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 3 | ||
rs2285810 | 12 | 112261736 | non coding transcript exon variant | T/C | snv | 0.45 | 2 | ||||
rs4766898 | 12 | 112344040 | intron variant | C/T | snv | 4.8E-02 | 1 | ||||
rs77768175 | 1.000 | 0.040 | 12 | 112298314 | intron variant | A/G | snv | 5.8E-03 | 1 | ||
rs1005902 | 12 | 112229871 | missense variant | T/C;G | snv | 4.1E-06; 0.42 | 1 | ||||
rs11066194 | 1.000 | 0.040 | 12 | 112212323 | intron variant | A/G | snv | 4.8E-02 | 1 | ||
rs2301712 | 12 | 112203573 | non coding transcript exon variant | T/G | snv | 0.10 | 9.1E-02 | 1 |