Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4804833 | 1.000 | 0.040 | 19 | 7905750 | intron variant | A/G;T | snv | 1 | |||
rs4795942 | 1.000 | 0.040 | 17 | 34584149 | intron variant | C/T | snv | 0.72 | 1 | ||
rs4760820 | 0.925 | 0.040 | 12 | 72003216 | intron variant | C/G | snv | 0.29 | 2 | ||
rs4746 | 0.708 | 0.400 | 6 | 38682852 | missense variant | T/A;G | snv | 0.36 | 21 | ||
rs4722999 | 0.851 | 0.080 | 7 | 30654159 | intron variant | C/T | snv | 0.67 | 5 | ||
rs4684677 | 0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 | 13 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs4606 | 0.752 | 0.120 | 1 | 192812042 | 3 prime UTR variant | C/G;T | snv | 16 | |||
rs4583306 | 1.000 | 0.040 | 17 | 30211697 | intron variant | A/G | snv | 0.37 | 1 | ||
rs4570625 | 0.724 | 0.200 | 12 | 71938143 | upstream gene variant | G/T | snv | 0.27 | 25 | ||
rs4565946 | 0.827 | 0.080 | 12 | 71942989 | intron variant | C/A;G;T | snv | 7 | |||
rs4448731 | 1.000 | 0.040 | 12 | 71935326 | upstream gene variant | T/C | snv | 0.40 | 1 | ||
rs4145262 | 1.000 | 0.040 | 12 | 105659532 | regulatory region variant | C/A | snv | 4.8E-02 | 1 | ||
rs4076452 | 1.000 | 0.040 | 17 | 45778528 | intron variant | G/C | snv | 0.16 | 2 | ||
rs3816995 | 1.000 | 0.040 | 17 | 73339121 | intron variant | G/A | snv | 0.40 | 1 | ||
rs3813034 | 0.827 | 0.160 | 17 | 30197786 | 3 prime UTR variant | A/C | snv | 0.40 | 8 | ||
rs37790 | 1.000 | 0.040 | 5 | 53346682 | intergenic variant | C/G;T | snv | 1 | |||
rs3749034 | 0.827 | 0.040 | 2 | 170816965 | 5 prime UTR variant | G/A;T | snv | 6 | |||
rs3742278 | 1.000 | 0.040 | 13 | 46845442 | intron variant | A/G | snv | 0.19 | 1 | ||
rs324981 | 0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 | 18 | |
rs324891 | 1.000 | 0.040 | 5 | 88616114 | intron variant | C/T | snv | 4.2E-04 | 1 | ||
rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
rs3219151 | 0.752 | 0.160 | 5 | 161701908 | 3 prime UTR variant | C/T | snv | 0.51 | 14 | ||
rs3213207 | 0.776 | 0.120 | 6 | 15627871 | intron variant | T/C | snv | 8.7E-02 | 11 | ||
rs2910931 | 0.925 | 0.080 | 5 | 32394809 | intron variant | T/A | snv | 0.63 | 3 |