Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 6 | ||||
rs113525195 | 14 | 23030112 | intron variant | C/A;T | snv | 2 | |||||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs113700287 | 3 | 24293020 | intron variant | -/GTT | delins | 4 | |||||
rs113809617 | 9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 | 5 | |||
rs11771301 | 7 | 5195031 | intron variant | C/G;T | snv | 2 | |||||
rs140446749 | 1 | 158668470 | intron variant | G/A | snv | 8.0E-03 | 2 | ||||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 10 | |||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 5 | ||||
rs146771786 | 6 | 16285830 | missense variant | C/A | snv | 1.3E-03 | 1.3E-03 | 2 | |||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 6 | ||||
rs159058 | 20 | 32520305 | intron variant | A/C;T | snv | 4 | |||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 6 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 11 | |||||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 9 | ||||
rs2227930 | 3 | 142558733 | synonymous variant | A/T | snv | 0.55 | 0.63 | 2 | |||
rs2748424 | 17 | 78128784 | intron variant | C/G | snv | 0.26 | 4 | ||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 4 | ||||
rs35259020 | 9 | 134085798 | intergenic variant | CT/- | delins | 0.18 | 3 | ||||
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 | |||
rs4832312 | 2 | 86762839 | intron variant | G/A;C | snv | 3 | |||||
rs532398216 | 16 | 182398 | downstream gene variant | TGAG/- | delins | 2.0E-03 | 5 |