Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6750228 | 2 | 51084986 | intron variant | T/A | snv | 6.9E-02 | 1 | ||||
rs6768627 | 3 | 46853886 | intron variant | C/T | snv | 0.13 | 1 | ||||
rs7654754 | 4 | 76488642 | intron variant | G/A | snv | 0.43 | 1 | ||||
rs7670121 | 4 | 148207444 | intron variant | A/G | snv | 0.24 | 1 | ||||
rs7731168 | 5 | 65000644 | intron variant | G/C | snv | 0.29 | 1 | ||||
rs8035855 | 15 | 41785763 | intron variant | G/A | snv | 0.59 | 1 | ||||
rs2472297 | 0.882 | 0.160 | 15 | 74735539 | intergenic variant | C/T | snv | 0.16 | 5 | ||
rs12032996 | 1 | 33454985 | intergenic variant | G/A | snv | 0.12 | 1 | ||||
rs12727104 | 1 | 171454028 | intergenic variant | G/A | snv | 8.3E-02 | 1 | ||||
rs13394343 | 2 | 85527219 | intergenic variant | C/A;T | snv | 1 | |||||
rs183131780 | 2 | 225820170 | intergenic variant | C/T | snv | 1.0E-03 | 1 | ||||
rs185291443 | 2 | 226120788 | intergenic variant | C/A;G | snv | 1 | |||||
rs35311980 | 2 | 228295484 | intergenic variant | C/T | snv | 4.9E-05 | 1 | ||||
rs35924503 | 2 | 228266570 | intergenic variant | T/C | snv | 1.5E-04 | 1 | ||||
rs4288924 | 14 | 68835682 | intergenic variant | G/A;T | snv | 1 | |||||
rs6712846 | 2 | 207024356 | intergenic variant | G/A | snv | 0.53 | 1 | ||||
rs17158386 | 7 | 29765745 | regulatory region variant | G/A | snv | 0.19 | 2 | ||||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs10995311 | 10 | 62805174 | missense variant | C/G | snv | 0.35 | 0.31 | 3 | |||
rs2236295 | 10 | 62805132 | missense variant | G/C;T | snv | 0.32 | 2 | ||||
rs45551835 | 1.000 | 0.080 | 10 | 16890385 | missense variant | G/A;T | snv | 1.3E-02; 4.0E-06 | 2 | ||
rs141640975 | 10 | 16950012 | missense variant | G/A | snv | 1.7E-03 | 1.5E-03 | 1 | |||
rs144360241 | 10 | 16925418 | missense variant | T/C | snv | 5.6E-03 | 5.3E-03 | 1 | |||
rs144994089 | 9 | 33385158 | missense variant | C/T | snv | 7.0E-04 | 8.2E-04 | 1 | |||
rs1801239 | 0.827 | 0.160 | 10 | 16877053 | missense variant | T/C;G | snv | 8.9E-02; 8.0E-06 | 1 |