Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6756667 | 1.000 | 0.040 | 2 | 46352270 | intron variant | A/G | snv | 0.62 | 1 | ||
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs4353747 | 1.000 | 0.040 | 22 | 30630488 | downstream gene variant | C/A;T | snv | 1 | |||
rs7292407 | 1.000 | 0.040 | 22 | 46057832 | non coding transcript exon variant | C/A;T | snv | 1 | |||
rs2229616 | 0.732 | 0.200 | 18 | 60372043 | missense variant | C/T | snv | 1.6E-02 | 1.6E-02 | 22 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs2254298 | 0.701 | 0.200 | 3 | 8760542 | intron variant | G/A | snv | 0.16 | 23 | ||
rs800629 | 0.882 | 0.120 | 2 | 37752757 | intergenic variant | G/A | snv | 3 | |||
rs4253747 | 1.000 | 0.040 | 22 | 46217340 | intron variant | T/A | snv | 0.30 | 1 | ||
rs6520015 | 1.000 | 0.040 | 22 | 46067551 | non coding transcript exon variant | T/A;C | snv | 1 |