Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113700287 | 3 | 24293020 | intron variant | -/GTT | delins | 4 | |||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 4 | ||||
rs592423 | 6 | 139519556 | intron variant | A/C | snv | 0.50 | 5 | ||||
rs754205 | 13 | 109759295 | intron variant | A/C;G | snv | 4 | |||||
rs159058 | 20 | 32520305 | intron variant | A/C;T | snv | 4 | |||||
rs61823972 | 1 | 205232197 | intron variant | A/C;T | snv | 4 | |||||
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 6 | ||||
rs8013143 | 14 | 23025068 | intron variant | A/G | snv | 0.43 | 4 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs2227930 | 3 | 142558733 | synonymous variant | A/T | snv | 0.55 | 0.63 | 2 | |||
rs706027 | 7 | 16660352 | intron variant | A/T | snv | 0.43 | 4 | ||||
rs146771786 | 6 | 16285830 | missense variant | C/A | snv | 1.3E-03 | 1.3E-03 | 2 | |||
rs113525195 | 14 | 23030112 | intron variant | C/A;T | snv | 2 | |||||
rs113809617 | 9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 | 5 | |||
rs2748424 | 17 | 78128784 | intron variant | C/G | snv | 0.26 | 4 | ||||
rs11771301 | 7 | 5195031 | intron variant | C/G;T | snv | 2 | |||||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
rs6600233 | 16 | 93505 | intron variant | C/G;T | snv | 2 | |||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 5 | ||||
rs35788208 | 5 | 154654616 | intergenic variant | C/T | snv | 7.4E-02 | 2 | ||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 20 | |
rs35259020 | 9 | 134085798 | intergenic variant | CT/- | delins | 0.18 | 3 | ||||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs140446749 | 1 | 158668470 | intron variant | G/A | snv | 8.0E-03 | 2 |