Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 11 | |||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 10 | ||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 7 | ||||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 7 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 7 | ||
rs737092 | 20 | 57415349 | regulatory region variant | T/C | snv | 0.58 | 7 | ||||
rs8887 | 1.000 | 0.080 | 19 | 4502189 | 3 prime UTR variant | T/C;G | snv | 0.51; 1.8E-05 | 7 | ||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 7 | |||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
rs592423 | 6 | 139519556 | intron variant | A/C | snv | 0.50 | 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 | |||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 5 | ||||
rs4434553 | 1.000 | 0.040 | 7 | 100642568 | intron variant | A/G | snv | 0.40 | 5 | ||
rs532398216 | 16 | 182398 | downstream gene variant | TGAG/- | delins | 2.0E-03 | 5 | ||||
rs113700287 | 3 | 24293020 | intron variant | -/GTT | delins | 4 | |||||
rs159058 | 20 | 32520305 | intron variant | A/C;T | snv | 4 | |||||
rs2748424 | 17 | 78128784 | intron variant | C/G | snv | 0.26 | 4 | ||||
rs61823972 | 1 | 205232197 | intron variant | A/C;T | snv | 4 |