Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10484566 | 0.925 | 0.200 | 6 | 32867481 | regulatory region variant | T/G | snv | 6.8E-02 | 2 | ||
rs10795791 | 0.925 | 0.200 | 10 | 6066377 | upstream gene variant | A/G | snv | 0.40 | 2 | ||
rs1214611 | 0.925 | 0.200 | 1 | 167479867 | intron variant | A/G | snv | 0.54 | 2 | ||
rs12177980 | 0.925 | 0.200 | 6 | 32718307 | non coding transcript exon variant | G/A | snv | 0.37 | 2 | ||
rs154981 | 0.925 | 0.200 | 6 | 32913216 | regulatory region variant | C/A;G;T | snv | 2 | |||
rs2027856 | 0.925 | 0.200 | 6 | 32434928 | upstream gene variant | G/A | snv | 0.18 | 2 | ||
rs2050189 | 0.925 | 0.200 | 6 | 32371870 | 5 prime UTR variant | T/C;G | snv | 0.18 | 2 | ||
rs206015 | 0.925 | 0.200 | 6 | 32214982 | intron variant | G/A | snv | 0.15 | 2 | ||
rs2064478 | 0.925 | 0.200 | 6 | 33104489 | intron variant | C/T | snv | 0.28 | 2 | ||
rs2071540 | 0.925 | 0.200 | 6 | 32845139 | non coding transcript exon variant | T/C | snv | 0.61 | 2 | ||
rs2071554 | 0.925 | 0.200 | 6 | 32816899 | missense variant | C/A;T | snv | 4.1E-06; 6.2E-02 | 2 | ||
rs2076537 | 0.925 | 0.200 | 6 | 32349858 | non coding transcript exon variant | G/A | snv | 0.37 | 0.42 | 2 | |
rs2256965 | 0.925 | 0.200 | 6 | 31587353 | non coding transcript exon variant | A/G;T | snv | 0.60 | 2 | ||
rs2267644 | 0.925 | 0.200 | 6 | 32224783 | upstream gene variant | G/A | snv | 4.9E-02 | 2 | ||
rs2280800 | 0.925 | 0.200 | 6 | 31678621 | intron variant | C/A | snv | 0.14 | 2 | ||
rs2395150 | 0.925 | 0.200 | 6 | 32358268 | intron variant | G/A | snv | 0.51 | 2 | ||
rs2395162 | 0.925 | 0.200 | 6 | 32420003 | intergenic variant | G/T | snv | 0.13 | 2 | ||
rs2395175 | 0.925 | 0.200 | 6 | 32437249 | upstream gene variant | G/A | snv | 0.12 | 2 | ||
rs241407 | 0.925 | 0.200 | 6 | 32894963 | upstream gene variant | C/T | snv | 9.7E-02 | 2 | ||
rs241409 | 0.925 | 0.200 | 6 | 32894143 | upstream gene variant | A/G | snv | 9.8E-02 | 2 | ||
rs241424 | 0.925 | 0.200 | 6 | 32837157 | intron variant | G/A | snv | 0.50 | 2 | ||
rs2516440 | 0.925 | 0.200 | 6 | 31472720 | intron variant | G/A | snv | 0.41 | 2 | ||
rs2844533 | 0.925 | 0.200 | 6 | 31383025 | upstream gene variant | G/A | snv | 0.74 | 2 | ||
rs2844746 | 0.925 | 0.200 | 6 | 30371825 | intergenic variant | T/C | snv | 0.69 | 2 | ||
rs3129962 | 0.925 | 0.200 | 6 | 32411606 | upstream gene variant | G/A;C | snv | 2 |