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 | ||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 11 | ||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 9 | ||
rs2470893 | 0.882 | 0.160 | 15 | 74727108 | upstream gene variant | C/T | snv | 0.20 | 8 | ||
rs1613662 | 0.851 | 0.120 | 19 | 55025227 | missense variant | G/A | snv | 0.85 | 0.83 | 8 | |
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 6 | |||||
rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 | ||||
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 5 | ||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs8176685 | 9 | 133263363 | intron variant | CACCACTACGCC/- | delins | 4 | |||||
rs74847330 | 2 | 143074030 | intergenic variant | A/G | snv | 8.8E-02 | 4 | ||||
rs56043070 | 1 | 247556467 | splice donor variant | G/A;T | snv | 5.2E-02; 4.1E-06 | 4 | ||||
rs4432538 | 20 | 8626746 | intron variant | G/A | snv | 0.52 | 4 | ||||
rs374039502 | 0.925 | 0.160 | 13 | 108308037 | 3 prime UTR variant | T/A | snv | 2.0E-02 | 4 | ||
rs117672662 | 14 | 68958750 | intron variant | T/C | snv | 7.4E-03 | 3 | ||||
rs17572109 | 2 | 218229211 | non coding transcript exon variant | G/A;T | snv | 3 | |||||
rs2901656 | 1 | 172465672 | 3 prime UTR variant | C/A;T | snv | 0.51 | 3 | ||||
rs553749201 | 17 | 4933900 | synonymous variant | C/A | snv | 3 | |||||
rs139141690 | 7 | 101856650 | intron variant | G/A | snv | 2.2E-03 | 3 | ||||
rs655029 | 2 | 31254972 | intron variant | G/A | snv | 0.78 | 3 | ||||
rs41315846 | 1 | 247549001 | intron variant | T/C | snv | 0.44 | 0.52 | 3 | |||
rs10886430 | 10 | 119250744 | intron variant | A/G | snv | 8.8E-02 | 3 |