Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 7 | ||||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 25 | ||
rs55791371 | 0.925 | 0.080 | 19 | 11077477 | intron variant | A/C | snv | 0.11 | 3 | ||
rs17249141 | 19 | 11089332 | upstream gene variant | C/T | snv | 3.3E-03 | 4 | ||||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 15 | ||
rs651821 | 0.851 | 0.360 | 11 | 116791863 | 5 prime UTR variant | C/T | snv | 0.88 | 0.89 | 17 | |
rs6982636 | 8 | 125467073 | intron variant | G/A | snv | 0.43 | 7 | ||||
rs11075253 | 16 | 15054789 | intron variant | C/A | snv | 0.22 | 1 | ||||
rs11644601 | 16 | 15078261 | intron variant | T/C | snv | 0.21 | 4 | ||||
rs67418890 | 1 | 161571067 | intron variant | T/A;C | snv | 1 | |||||
rs190121281 | 19 | 19141970 | upstream gene variant | G/A | snv | 3.5E-03 | 1 | ||||
rs331 | 8 | 19962894 | intron variant | G/A | snv | 0.30 | 4 | ||||
rs1059611 | 8 | 19967052 | 3 prime UTR variant | T/C | snv | 0.13 | 3 | ||||
rs115849089 | 8 | 20054859 | intergenic variant | G/A | snv | 9.8E-02 | 7 | ||||
rs6754295 | 1.000 | 0.040 | 2 | 20983311 | regulatory region variant | T/G | snv | 0.27 | 6 | ||
rs676210 | 0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 | 12 | ||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 14 | |||
rs12713956 | 2 | 21018633 | intron variant | A/G | snv | 0.14 | 4 | ||||
rs1367117 | 1.000 | 0.080 | 2 | 21041028 | missense variant | G/A | snv | 0.26 | 0.24 | 8 | |
rs312985 | 2 | 21155933 | regulatory region variant | A/G | snv | 0.75 | 2 | ||||
rs506585 | 2 | 21174310 | intergenic variant | G/A;C;T | snv | 4 | |||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs6917603 | 6 | 30049294 | intron variant | T/C | snv | 0.15 | 2 | ||||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 11 | |||
rs4245791 | 0.882 | 0.080 | 2 | 43847292 | non coding transcript exon variant | C/A;T | snv | 8 |