Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 11 | |||||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 10 | ||||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 9 | ||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 8 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs112875651 | 8 | 125494452 | intron variant | G/A | snv | 0.31 | 7 | ||||
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 6 | ||||
rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 | ||||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 6 | ||||
rs415895 | 11 | 9748015 | missense variant | C/G | snv | 0.62 | 0.61 | 6 | |||
rs4737010 | 8 | 41772929 | intron variant | G/A | snv | 0.32 | 6 | ||||
rs7133378 | 12 | 123924955 | intron variant | G/A | snv | 0.38 | 6 | ||||
rs737092 | 20 | 57415349 | regulatory region variant | T/C | snv | 0.58 | 6 | ||||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 6 | |||||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs113809617 | 9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 | 5 | |||
rs1175550 | 1 | 3774964 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 5 | ||||
rs2022003 | 1 | 158617176 | intron variant | A/T | snv | 0.28 | 5 | ||||
rs532398216 | 16 | 182398 | downstream gene variant | TGAG/- | delins | 2.0E-03 | 5 | ||||
rs592423 | 6 | 139519556 | intron variant | A/C | snv | 0.50 | 5 | ||||
rs74035509 | 16 | 88500925 | intron variant | C/T | snv | 0.10 | 5 |