Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2293157 | 0.763 | 0.120 | 17 | 42300657 | intron variant | C/A;T | snv | 9 | |||
rs1494555 | 0.790 | 0.120 | 5 | 35871088 | missense variant | G/A | snv | 0.64 | 0.72 | 8 | |
rs1057519825 | 0.882 | 0.120 | X | 101356176 | missense variant | C/G | snv | 7 | |||
rs1057519826 | 0.882 | 0.120 | X | 101356177 | missense variant | A/T | snv | 7 | |||
rs9392504 | 0.827 | 0.120 | 6 | 412802 | downstream gene variant | G/A | snv | 0.44 | 7 | ||
rs4985726 | 0.925 | 0.120 | 17 | 16960324 | intron variant | C/G | snv | 0.11 | 5 | ||
rs11866002 | 0.851 | 0.120 | 16 | 58553833 | synonymous variant | C/T | snv | 0.35 | 0.39 | 4 | |
rs3755397 | 0.925 | 0.120 | 2 | 241355498 | upstream gene variant | A/G | snv | 6.8E-02 | 4 | ||
rs1057519831 | 1.000 | 0.120 | 16 | 81912655 | missense variant | C/T | snv | 3 | |||
rs139996880 | 0.882 | 0.120 | 5 | 1284538 | intron variant | G/A | snv | 0.12 | 3 | ||
rs210134 | 1.000 | 0.120 | 6 | 33572432 | intron variant | A/G | snv | 0.72 | 3 | ||
rs210142 | 0.925 | 0.120 | 6 | 33579060 | intron variant | T/C | snv | 0.74 | 3 | ||
rs2292982 | 1.000 | 0.120 | 16 | 85911217 | intron variant | T/C;G | snv | 3 | |||
rs35923643 | 0.925 | 0.120 | 11 | 123484683 | intron variant | A/G | snv | 0.15 | 3 | ||
rs4987852 | 0.925 | 0.120 | 18 | 63126688 | 3 prime UTR variant | T/C | snv | 5.1E-02 | 3 | ||
rs9815073 | 0.925 | 0.120 | 3 | 188397894 | intron variant | C/A;G | snv | 3 | |||
rs1036935 | 0.925 | 0.120 | 18 | 50317164 | upstream gene variant | A/G;T | snv | 2 | |||
rs1044873 | 0.925 | 0.120 | 16 | 85922065 | 3 prime UTR variant | C/T | snv | 0.40 | 2 | ||
rs11636802 | 0.925 | 0.120 | 15 | 56483399 | intergenic variant | A/G | snv | 8.0E-02 | 2 | ||
rs11637565 | 0.925 | 0.120 | 15 | 69728186 | intron variant | G/A | snv | 0.66 | 2 | ||
rs1274963 | 0.925 | 0.120 | 3 | 39149538 | non coding transcript exon variant | A/G | snv | 0.82 | 2 | ||
rs13015798 | 0.925 | 0.120 | 2 | 201044792 | intron variant | A/G | snv | 0.23 | 2 | ||
rs13401811 | 0.925 | 0.120 | 2 | 110858527 | intron variant | G/A | snv | 0.19 | 2 | ||
rs1359742 | 0.925 | 0.120 | 9 | 22336997 | intergenic variant | G/C;T | snv | 2 | |||
rs1373425060 | 0.925 | 0.120 | 9 | 4719290 | missense variant | G/C | snv | 4.0E-06 | 2 |