Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4754 | 0.752 | 0.360 | 4 | 87981540 | missense variant | T/A;C | snv | 0.32 | 12 | ||
rs9138 | 0.776 | 0.360 | 4 | 87983190 | 3 prime UTR variant | A/C;T | snv | 12 | |||
rs11730582 | 0.807 | 0.240 | 4 | 87975269 | non coding transcript exon variant | T/C | snv | 0.37 | 10 | ||
rs1126616 | 0.827 | 0.280 | 4 | 87982701 | synonymous variant | C/G;T | snv | 0.32 | 0.26 | 8 | |
rs1126772 | 0.851 | 0.320 | 4 | 87983034 | 3 prime UTR variant | A/G | snv | 0.16 | 5 | ||
rs17524488 | 0.925 | 0.040 | 4 | 87975555 | non coding transcript exon variant | -/G | delins | 4 | |||
rs2853744 | 0.882 | 0.200 | 4 | 87975096 | non coding transcript exon variant | G/T | snv | 0.14 | 4 | ||
rs2728127 | 0.882 | 0.120 | 4 | 87973963 | upstream gene variant | A/G;T | snv | 3 | |||
rs28357094 | 0.882 | 0.160 | 4 | 87975645 | non coding transcript exon variant | T/G | snv | 0.17 | 3 | ||
rs11728697 | 0.925 | 0.080 | 4 | 87977789 | non coding transcript exon variant | C/T | snv | 0.54 | 0.46 | 2 | |
rs11439060 | 1.000 | 0.120 | 4 | 87975555 | non coding transcript exon variant | -/G | delins | 1 | |||
rs2853749 | 0.882 | 0.160 | 4 | 87976662 | intron variant | C/T | snv | 0.34 | 1 | ||
rs1370031102 | 1.000 | 0.080 | 4 | 87982700 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 |