Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10892279 | 1.000 | 0.120 | 11 | 118741072 | intron variant | G/A;T | snv | 0.25 | 3 | ||
rs1953126 | 1.000 | 0.120 | 9 | 120878222 | intron variant | T/C | snv | 0.68 | 2 | ||
rs13031237 | 1.000 | 0.120 | 2 | 60908994 | intron variant | G/T | snv | 0.25 | 1 | ||
rs17066096 | 1.000 | 0.080 | 6 | 137131771 | intergenic variant | A/G | snv | 0.20 | 1 | ||
rs2108225 | 1.000 | 0.040 | 7 | 107812658 | downstream gene variant | G/A;T | snv | 1 | |||
rs212402 | 1.000 | 0.080 | 6 | 159051263 | intron variant | G/A | snv | 0.66 | 1 | ||
rs2280141 | 1.000 | 0.040 | 10 | 122433665 | 3 prime UTR variant | T/G | snv | 0.56 | 1 | ||
rs4648356 | 1.000 | 0.080 | 1 | 2792599 | intron variant | C/A | snv | 0.39 | 1 | ||
rs6726160 | 1.000 | 0.080 | 2 | 60937594 | non coding transcript exon variant | T/G | snv | 0.47 | 1 | ||
rs6848139 | 1.000 | 0.040 | 4 | 122473886 | intergenic variant | A/C;G | snv | 1 | |||
rs7523907 | 1.000 | 0.080 | 1 | 167458010 | non coding transcript exon variant | C/A;T | snv | 1 | |||
rs1131017 | 0.925 | 0.160 | 12 | 56042145 | 5 prime UTR variant | C/A;G;T | snv | 8.0E-06; 8.0E-06; 0.62; 1.1E-04 | 3 | ||
rs6933404 | 0.925 | 0.280 | 6 | 137638098 | intergenic variant | T/C | snv | 0.16 | 3 | ||
rs864537 | 0.925 | 0.200 | 1 | 167442147 | intron variant | A/G | snv | 0.29 | 3 | ||
rs2281808 | 0.925 | 0.160 | 20 | 1629905 | intron variant | T/A;C | snv | 2 | |||
rs2456973 | 0.925 | 0.040 | 12 | 56023144 | intron variant | A/C;G | snv | 2 | |||
rs3890745 | 0.925 | 0.200 | 1 | 2622185 | intron variant | T/C | snv | 0.40 | 2 | ||
rs6859219 | 0.925 | 0.160 | 5 | 56142753 | intron variant | C/A | snv | 0.20 | 2 | ||
rs10892258 | 0.925 | 0.120 | 11 | 118709156 | intron variant | G/A | snv | 0.19 | 1 | ||
rs11676922 | 0.925 | 0.160 | 2 | 100190478 | intron variant | T/A | snv | 0.51 | 1 | ||
rs13315591 | 0.925 | 0.160 | 3 | 58571114 | intron variant | T/C | snv | 0.15 | 1 | ||
rs13390936 | 0.925 | 0.080 | 2 | 191090090 | intron variant | A/T | snv | 8.4E-02 | 1 | ||
rs1800907 | 0.925 | 0.120 | 7 | 142800425 | upstream gene variant | T/C | snv | 0.56 | 1 | ||
rs212389 | 0.925 | 0.160 | 6 | 159068759 | non coding transcript exon variant | G/A | snv | 0.60 | 1 | ||
rs231804 | 0.925 | 0.200 | 2 | 203843923 | intergenic variant | C/T | snv | 0.60 | 1 |