Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs31490 | 0.776 | 0.280 | 5 | 1344343 | splice region variant | G/A;T | snv | 0.37; 8.0E-06 | 2 | ||
rs757978 | 0.851 | 0.200 | 2 | 241431686 | missense variant | C/A;T | snv | 4.1E-06; 9.3E-02 | 2 | ||
rs11668878 | 0.925 | 0.200 | 19 | 46765116 | intron variant | G/T | snv | 5.1E-02 | 2 | ||
rs1050976 | 0.851 | 0.280 | 6 | 408079 | 3 prime UTR variant | C/T | snv | 0.37 | 2 | ||
rs391525 | 0.882 | 0.200 | 16 | 85910833 | intron variant | A/G;T | snv | 0.35 | 2 | ||
rs11083846 | 0.882 | 0.200 | 19 | 46704397 | splice region variant | G/A | snv | 0.17 | 0.16 | 2 | |
rs3803800 | 0.807 | 0.240 | 17 | 7559652 | missense variant | A/G | snv | 0.70 | 0.64 | 2 | |
rs13069553 | 0.851 | 0.200 | 3 | 169790484 | upstream gene variant | A/G | snv | 0.21 | 1 | ||
rs1359742 | 0.925 | 0.120 | 9 | 22336997 | intergenic variant | G/C;T | snv | 1 | |||
rs1679013 | 0.882 | 0.160 | 9 | 22206988 | intron variant | C/A;T | snv | 0.43 | 1 | ||
rs2511714 | 0.925 | 0.120 | 8 | 102566646 | regulatory region variant | T/G | snv | 0.41 | 1 | ||
rs35748167 | 1.000 | 0.120 | 18 | 60370200 | intron variant | G/C;T | snv | 1 | |||
rs391023 | 0.925 | 0.120 | 16 | 85894208 | upstream gene variant | C/T | snv | 0.48 | 1 | ||
rs4368253 | 0.925 | 0.120 | 18 | 59955055 | TF binding site variant | T/A;C | snv | 1 | |||
rs674313 | 0.925 | 0.120 | 6 | 32610305 | intergenic variant | C/T | snv | 0.29 | 1 | ||
rs7944004 | 0.925 | 0.120 | 11 | 2289922 | intergenic variant | T/G | snv | 0.48 | 1 | ||
rs8024033 | 0.925 | 0.120 | 15 | 40111456 | upstream gene variant | C/G | snv | 0.50 | 1 | ||
rs13401811 | 0.925 | 0.120 | 2 | 110858527 | intron variant | G/A | snv | 0.19 | 1 | ||
rs1439287 | 0.925 | 0.120 | 2 | 111114320 | non coding transcript exon variant | G/A | snv | 0.42 | 1 | ||
rs1800682 | 0.637 | 0.440 | 10 | 88990206 | non coding transcript exon variant | A/G | snv | 0.54 | 1 | ||
rs4987852 | 0.925 | 0.120 | 18 | 63126688 | 3 prime UTR variant | T/C | snv | 5.1E-02 | 1 | ||
rs4987855 | 0.925 | 0.120 | 18 | 63126316 | 3 prime UTR variant | C/T | snv | 5.9E-02 | 1 | ||
rs4987856 | 0.925 | 0.120 | 18 | 63126261 | 3 prime UTR variant | C/T | snv | 6.0E-02 | 1 | ||
rs6858698 | 0.925 | 0.120 | 4 | 113762688 | upstream gene variant | G/C | snv | 0.20 | 1 | ||
rs2466032 | 1.000 | 0.120 | 8 | 127197575 | non coding transcript exon variant | T/C | snv | 0.23 | 1 |