Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34608001 | 0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 | 5 | |
rs4988483 | 0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 | 11 | |
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs2839350 | 0.827 | 0.080 | 21 | 46597307 | downstream gene variant | G/A | snv | 0.22 | 5 | ||
rs3788266 | 0.732 | 0.160 | 21 | 46606442 | upstream gene variant | G/A | snv | 0.50 | 12 | ||
rs2076137 | 0.807 | 0.080 | 22 | 50077337 | intron variant | C/T | snv | 0.14 | 6 | ||
rs2235349 | 0.807 | 0.080 | 22 | 50079810 | intron variant | T/C | snv | 0.22 | 6 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 |