Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4246905 | 0.716 | 0.400 | 9 | 114790969 | missense variant | T/A;C | snv | 0.76 | 15 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs12928404 | 0.724 | 0.240 | 16 | 28835925 | splice region variant | T/C | snv | 0.44 | 0.45 | 15 | |
rs602662 | 0.716 | 0.280 | 19 | 48703728 | missense variant | G/A | snv | 0.40 | 0.47 | 15 | |
rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 7 | ||
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs10988542 | 0.724 | 0.240 | 9 | 129894985 | intron variant | G/A;C | snv | 14 | |||
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 8 | |||
rs114846446 | 0.724 | 0.240 | 2 | 2944140 | intron variant | G/A | snv | 9.5E-03 | 14 | ||
rs11580078 | 0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv | 14 | |||
rs117372389 | 0.724 | 0.240 | 16 | 50634166 | 3 prime UTR variant | G/T | snv | 1.1E-02 | 14 | ||
rs11741255 | 0.724 | 0.240 | 5 | 132475490 | intron variant | G/A | snv | 0.29 | 14 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 15 | ||
rs1250563 | 0.724 | 0.240 | 10 | 79287626 | intron variant | G/C | snv | 0.24 | 14 | ||
rs12598357 | 0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 | 15 | ||
rs12863738 | 0.724 | 0.240 | X | 136949968 | intron variant | C/T | snv | 0.16 | 14 | ||
rs13003464 | 0.827 | 0.200 | 2 | 60959694 | intron variant | A/G | snv | 0.50 | 3 | ||
rs13132308 | 0.807 | 0.160 | 4 | 122629959 | intron variant | A/G | snv | 0.10 | 6 | ||
rs1332099 | 0.724 | 0.240 | 10 | 99538694 | downstream gene variant | T/C;G | snv | 14 | |||
rs1689510 | 0.724 | 0.240 | 12 | 56002984 | non coding transcript exon variant | G/C | snv | 0.25 | 16 | ||
rs17466626 | 0.724 | 0.240 | 12 | 40366829 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 14 | ||
rs17885785 | 0.724 | 0.240 | 11 | 2146620 | non coding transcript exon variant | C/T | snv | 0.14 | 14 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 10 |