Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10454142 | 2 | 48419260 | intergenic variant | T/C | snv | 0.22 | 3 | ||||
rs10514317 | 5 | 89813933 | intergenic variant | C/A;T | snv | 3 | |||||
rs1573036 | X | 110576840 | intergenic variant | C/T | snv | 0.42 | 3 | ||||
rs1641537 | 17 | 7642403 | upstream gene variant | T/C | snv | 0.75 | 3 | ||||
rs17496332 | 1 | 107003753 | intergenic variant | A/G | snv | 0.26 | 3 | ||||
rs2411984 | 17 | 49368389 | intron variant | G/A | snv | 0.18 | 3 | ||||
rs293428 | 4 | 68726064 | intergenic variant | A/G | snv | 0.36 | 3 | ||||
rs3779195 | 7 | 98364050 | intron variant | T/A | snv | 0.16 | 3 | ||||
rs440837 | 8 | 80549739 | intergenic variant | A/G | snv | 0.39 | 3 | ||||
rs7910927 | 10 | 63379150 | intron variant | T/A;G | snv | 3 | |||||
rs8023580 | 15 | 96165062 | intron variant | T/C | snv | 0.29 | 3 | ||||
rs9901675 | 17 | 7581494 | missense variant | G/A | snv | 5.4E-02 | 5.5E-02 | 5 | |||
rs12150660 | 1.000 | 0.040 | 17 | 7618597 | intron variant | G/T | snv | 0.17 | 5 | ||
rs6258 | 1.000 | 0.040 | 17 | 7631360 | missense variant | C/A;T | snv | 5.6E-05; 4.5E-03 | 5 | ||
rs1625895 | 0.752 | 0.200 | 17 | 7674797 | non coding transcript exon variant | T/A;C;G | snv | 9.1E-06; 0.86; 4.5E-06 | 13 | ||
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 11 | ||
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 30 | ||
rs4149056 | 0.633 | 0.480 | 12 | 21178615 | missense variant | T/C | snv | 0.13 | 0.12 | 45 |