Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs113809617 | 9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 | 5 | |||
rs61823972 | 1 | 205232197 | intron variant | A/C;T | snv | 4 | |||||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 7 | ||||
rs4434553 | 1.000 | 0.040 | 7 | 100642568 | intron variant | A/G | snv | 0.40 | 5 | ||
rs415895 | 11 | 9748015 | missense variant | C/G | snv | 0.62 | 0.61 | 6 | |||
rs2022003 | 1 | 158617176 | intron variant | A/T | snv | 0.28 | 5 | ||||
rs1175550 | 1 | 3774964 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 5 | ||||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs1193 | 2 | 86775106 | 3 prime UTR variant | C/T | snv | 0.68 | 2 | ||||
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 7 | ||||
rs7853365 | 9 | 4855858 | intron variant | A/C;T | snv | 3 | |||||
rs13008603 | 2 | 46128709 | intron variant | C/A | snv | 0.10 | 5 | ||||
rs1357529 | 3 | 142632255 | intron variant | T/A;C;G | snv | 2 | |||||
rs8887 | 1.000 | 0.080 | 19 | 4502189 | 3 prime UTR variant | T/C;G | snv | 0.51; 1.8E-05 | 7 | ||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 11 | |||
rs60992881 | 16 | 107595 | intron variant | AAAAAAAAA/-;A;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAA | delins | 0.38 | 2 | ||||
rs6600233 | 16 | 93505 | intron variant | C/G;T | snv | 3 | |||||
rs59616136 | 19 | 17141231 | intron variant | G/A | snv | 8.1E-02 | 4 | ||||
rs7908745 | 10 | 45458319 | missense variant | A/G | snv | 0.31 | 0.33 | 2 | |||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs3896594 | 2 | 8622284 | intron variant | T/G | snv | 0.50 | 2 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 |