Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
rs204999 | 0.763 | 0.480 | 6 | 32142202 | intergenic variant | A/G | snv | 0.28 | 12 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 10 | |
rs9275572 | 0.724 | 0.360 | 6 | 32711222 | upstream gene variant | A/G;T | snv | 9 | |||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 8 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 8 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 7 | |
rs12663103 | 0.851 | 0.240 | 6 | 32193547 | intron variant | T/C | snv | 6.1E-02 | 7 | ||
rs477515 | 0.790 | 0.400 | 6 | 32601914 | intergenic variant | G/A | snv | 0.27 | 7 | ||
rs9275141 | 0.827 | 0.240 | 6 | 32683340 | intergenic variant | T/G | snv | 0.50 | 6 | ||
rs652888 | 0.776 | 0.480 | 6 | 31883457 | non coding transcript exon variant | A/G | snv | 0.18 | 0.20 | 6 | |
rs2395174 | 0.827 | 0.320 | 6 | 32437101 | upstream gene variant | T/G | snv | 0.24 | 5 | ||
rs2517459 | 0.882 | 0.160 | 6 | 30929245 | downstream gene variant | T/C | snv | 0.74 | 5 | ||
rs2856718 | 0.790 | 0.360 | 6 | 32702478 | downstream gene variant | C/T | snv | 0.34 | 5 | ||
rs3130542 | 0.827 | 0.160 | 6 | 31264334 | downstream gene variant | A/G | snv | 0.81 | 5 | ||
rs3130779 | 0.925 | 0.080 | 6 | 30904426 | upstream gene variant | A/C;G;T | snv | 5 | |||
rs1265115 | 0.925 | 0.080 | 6 | 31149298 | non coding transcript exon variant | C/A;T | snv | 5 | |||
rs3131034 | 0.925 | 0.080 | 6 | 30886019 | intron variant | G/A | snv | 0.75 | 5 | ||
rs9277554 | 0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 | 5 | ||
rs7453920 | 0.752 | 0.440 | 6 | 32762235 | intron variant | A/G;T | snv | 5 | |||
rs9268645 | 0.827 | 0.360 | 6 | 32440750 | intron variant | C/G;T | snv | 5 | |||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 5 | |
rs2596542 | 0.724 | 0.200 | 6 | 31398818 | upstream gene variant | C/T | snv | 0.41 | 5 |