Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1413711 | 0.882 | 0.200 | 6 | 43772941 | intron variant | T/A;C | snv | 3 | |||
rs833070 | 0.776 | 0.440 | 6 | 43774889 | non coding transcript exon variant | T/C | snv | 0.58 | 11 | ||
rs1005230 | 0.827 | 0.040 | 6 | 43768759 | upstream gene variant | T/C | snv | 0.60 | 5 | ||
rs3025021 | 0.882 | 0.160 | 6 | 43781426 | non coding transcript exon variant | T/C | snv | 0.70 | 4 | ||
rs374057152 | 0.925 | 0.200 | 6 | 43777592 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs1229919945 | 1.000 | 0.040 | 6 | 43782041 | missense variant | T/C | snv | 1 | |||
rs833069 | 0.851 | 0.200 | 6 | 43774842 | non coding transcript exon variant | T/C;G | snv | 5 | |||
rs3025010 | 6 | 43779840 | non coding transcript exon variant | T/C;G | snv | 1 | |||||
rs1188254133 | 0.851 | 0.240 | 6 | 43781990 | missense variant | T/G | snv | 7.0E-06 | 4 |