Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs3810291 | 19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 | 7 | ||||
rs11161721 | 1 | 86022231 | intron variant | C/A | snv | 0.27 | 0.27 | 4 | |||
rs4691380 | 4 | 156798972 | intron variant | C/T | snv | 0.45 | 4 | ||||
rs113722913 | 1 | 199950846 | intergenic variant | T/C | snv | 2.6E-02 | 3 | ||||
rs11847697 | 14 | 30045906 | intron variant | C/T | snv | 0.13 | 3 | ||||
rs13273088 | 8 | 69581739 | intron variant | G/A | snv | 0.81 | 3 | ||||
rs2300835 | 14 | 32738316 | intron variant | C/A | snv | 0.16 | 3 | ||||
rs2745353 | 6 | 127131790 | intron variant | C/T | snv | 0.55 | 3 | ||||
rs2785980 | 1 | 219527177 | intergenic variant | T/C | snv | 0.28 | 3 | ||||
rs308971 | 3 | 12075120 | intron variant | G/A | snv | 0.82 | 3 | ||||
rs35747 | 12 | 102518780 | intergenic variant | G/A | snv | 0.70 | 3 | ||||
rs4646949 | 6 | 34877672 | 3 prime UTR variant | T/C;G | snv | 3 | |||||
rs6689335 | 1 | 219455340 | intron variant | T/C | snv | 0.31 | 3 | ||||
rs731839 | 19 | 33408159 | intron variant | G/A | snv | 0.63 | 3 | ||||
rs8182584 | 19 | 33418804 | intron variant | T/C;G | snv | 3 | |||||
rs912056 | 6 | 6735964 | intron variant | A/T | snv | 0.66 | 3 | ||||
rs9552416 | 13 | 18737101 | downstream gene variant | C/A;T | snv | 3 | |||||
rs9841287 | 3 | 67310 | intergenic variant | A/G | snv | 0.22 | 3 | ||||
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 2 | ||||
rs11231693 | 11 | 64095140 | intron variant | G/A | snv | 0.11 | 2 | ||||
rs12714415 | 2 | 651430 | intergenic variant | T/C | snv | 0.19 | 2 | ||||
rs3822072 | 4 | 88820118 | intron variant | G/A;C | snv | 2 | |||||
rs4715210 | 6 | 50929538 | regulatory region variant | C/G;T | snv | 2 | |||||
rs4776970 | 15 | 67788548 | intron variant | A/T | snv | 0.44 | 2 |