Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8007267 | 0.882 | 0.200 | 14 | 54912273 | intergenic variant | C/T | snv | 0.31 | 6 | ||
rs10483639 | 1.000 | 0.040 | 14 | 54839739 | downstream gene variant | G/C | snv | 0.26 | 3 | ||
rs13361160 | 1.000 | 0.040 | 5 | 10169711 | downstream gene variant | T/C | snv | 0.34 | 2 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs6476030 | 1.000 | 0.040 | 9 | 289061 | intron variant | A/G | snv | 7.1E-02 | 1 | ||
rs6280 | 0.602 | 0.520 | 3 | 114171968 | missense variant | C/T | snv | 0.63 | 0.54 | 57 | |
rs3783641 | 0.882 | 0.120 | 14 | 54893421 | intron variant | T/A;C | snv | 0.25 | 4 | ||
rs12584920 | 1.000 | 0.040 | 13 | 46890902 | intron variant | G/C;T | snv | 1 | |||
rs1777971 | 1.000 | 0.040 | 6 | 58143645 | intron variant | A/G;T | snv | 1 | |||
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs563649 | 1.000 | 0.040 | 6 | 154086832 | 5 prime UTR variant | C/T | snv | 9.8E-02 | 2 | ||
rs6746030 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 16 |