Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs10889332 | 1.000 | 0.120 | 1 | 62485187 | 3 prime UTR variant | C/T | snv | 0.39 | 4 | ||
rs12040333 | 1.000 | 0.080 | 1 | 43848369 | intron variant | G/A;C | snv | 2 | |||
rs1998013 | 1 | 55492357 | intron variant | C/T | snv | 4.4E-03 | 1 | ||||
rs2390582 | 1 | 90478350 | intergenic variant | A/G | snv | 0.15 | 1 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 | |
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 14 | |||
rs10211524 | 2 | 64980940 | intron variant | G/A | snv | 0.51 | 4 | ||||
rs113533135 | 1.000 | 0.080 | 2 | 140268867 | intron variant | T/C | snv | 2.0E-02 | 2 | ||
rs1532002 | 1.000 | 0.080 | 2 | 140292500 | intron variant | G/A | snv | 2.3E-02 | 2 | ||
rs2680830 | 1.000 | 0.080 | 2 | 17596817 | intron variant | A/G;T | snv | 0.94 | 2 | ||
rs6754498 | 1.000 | 0.080 | 2 | 185953121 | non coding transcript exon variant | A/C;G;T | snv | 2 | |||
rs9973676 | 1.000 | 0.080 | 2 | 230954091 | intron variant | G/A | snv | 5.8E-02 | 2 | ||
rs749924 | 2 | 242084344 | upstream gene variant | C/T | snv | 0.25 | 1 | ||||
rs72928364 | 1.000 | 0.080 | 3 | 100894935 | intron variant | C/T | snv | 0.39 | 2 | ||
rs17404667 | 3 | 64288876 | intron variant | C/G | snv | 6.2E-02 | 1 | ||||
rs741013 | 3 | 64306961 | intron variant | A/T | snv | 6.0E-02 | 1 | ||||
rs1440581 | 1.000 | 0.080 | 4 | 88305270 | intron variant | T/A;C | snv | 4 | |||
rs1912826 | 4 | 186228386 | intron variant | G/A;C | snv | 4 | |||||
rs16850360 | 4 | 74006728 | intron variant | A/G | snv | 4.2E-02 | 2 | ||||
rs7442201 | 1.000 | 0.080 | 4 | 4360022 | intron variant | A/C;G | snv | 2 | |||
rs74570061 | 1.000 | 0.080 | 4 | 56517605 | intron variant | T/C | snv | 3.9E-02 | 2 | ||
rs76294234 | 1.000 | 0.080 | 4 | 83241025 | intron variant | A/G | snv | 1.5E-02 | 2 | ||
rs7689240 | 1.000 | 0.080 | 4 | 35313869 | intergenic variant | A/G | snv | 0.21 | 2 |