Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs56848936 | 0.776 | 0.080 | 19 | 45818249 | intron variant | A/G | snv | 1.9E-02 | 11 | ||
rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 10 | ||
rs2555639 | 0.851 | 0.080 | 4 | 174540379 | non coding transcript exon variant | T/C | snv | 0.38 | 7 | ||
rs719725 | 0.827 | 0.080 | 9 | 6365683 | intergenic variant | A/C | snv | 0.34 | 7 | ||
rs773442580 | 0.851 | 0.080 | 4 | 109913367 | missense variant | T/C;G | snv | 4.0E-06 | 7 | ||
rs1443465532 | 0.882 | 0.080 | 6 | 43774362 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs17878467 | 0.925 | 0.080 | 17 | 78214076 | upstream gene variant | C/G;T | snv | 6 | |||
rs5273 | 0.827 | 0.080 | 1 | 186674636 | missense variant | A/C;G | snv | 4.0E-06; 7.6E-03 | 1.4E-02 | 6 | |
rs60745952 | 0.925 | 0.080 | 4 | 148827842 | intron variant | T/C | snv | 0.13 | 6 | ||
rs6854845 | 0.827 | 0.080 | 4 | 74821455 | intergenic variant | G/T | snv | 0.13 | 6 | ||
rs1289280947 | 0.851 | 0.080 | 9 | 21974571 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
rs2853668 | 0.882 | 0.080 | 5 | 1299910 | upstream gene variant | G/T | snv | 0.33 | 5 | ||
rs35301225 | 0.882 | 0.080 | 1 | 9151743 | mature miRNA variant | C/A;T | snv | 5 | |||
rs3775292 | 0.851 | 0.080 | 4 | 186081871 | non coding transcript exon variant | C/G | snv | 0.82 | 5 | ||
rs4135113 | 0.925 | 0.080 | 12 | 103982915 | missense variant | G/A;C;T | snv | 4.7E-02 | 5 | ||
rs9365723 | 0.827 | 0.080 | 6 | 158014540 | intron variant | A/C;G | snv | 0.56 | 5 | ||
rs10222633 | 0.925 | 0.080 | 3 | 122258079 | intron variant | G/A | snv | 0.45 | 4 | ||
rs10934578 | 0.925 | 0.080 | 3 | 122258435 | intron variant | G/T | snv | 0.30 | 4 | ||
rs12591359 | 0.925 | 0.080 | 15 | 51247171 | intron variant | G/A | snv | 0.41 | 4 | ||
rs2737 | 0.851 | 0.080 | 17 | 47981705 | missense variant | T/C | snv | 0.25 | 0.19 | 4 | |
rs2770150 | 0.925 | 0.080 | 9 | 117700861 | upstream gene variant | A/G | snv | 0.22 | 4 | ||
rs3804513 | 0.851 | 0.080 | 6 | 52188399 | intron variant | A/T | snv | 2.4E-02 | 4 | ||
rs6588147 | 0.851 | 0.080 | 1 | 65469811 | intron variant | G/A | snv | 0.70 | 4 | ||
rs756363791 | 0.882 | 0.080 | 3 | 9756823 | missense variant | G/A | snv | 2.0E-05 | 4 | ||
rs7987649 | 0.925 | 0.080 | 13 | 28320278 | intron variant | A/G | snv | 0.35 | 4 |