Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 8 | ||||
rs10995311 | 10 | 62805174 | missense variant | C/G | snv | 0.35 | 0.31 | 3 | |||
rs112607182 | 3 | 170309619 | downstream gene variant | C/T | snv | 5.3E-02 | 2 | ||||
rs17158386 | 7 | 29765745 | regulatory region variant | G/A | snv | 0.19 | 2 | ||||
rs2236295 | 10 | 62805132 | missense variant | G/C;T | snv | 0.32 | 2 | ||||
rs6535594 | 4 | 148211605 | intron variant | G/A | snv | 0.54 | 2 | ||||
rs67339103 | 10 | 76133928 | intron variant | G/A;C;T | snv | 2 | |||||
rs10157710 | 1 | 47496019 | downstream gene variant | C/T | snv | 0.78 | 1 | ||||
rs10207567 | 2 | 202850250 | intron variant | G/A;C | snv | 1 | |||||
rs11162351 | 1 | 77479047 | intron variant | C/G | snv | 0.31 | 1 | ||||
rs1124694 | 11 | 11077129 | intron variant | A/G;T | snv | 1 | |||||
rs11264327 | 1 | 155122631 | downstream gene variant | G/A;C;T | snv | 1 | |||||
rs1145074 | 15 | 45411626 | intron variant | T/A;G | snv | 0.45 | 1 | ||||
rs12032996 | 1 | 33454985 | intergenic variant | G/A | snv | 0.12 | 1 | ||||
rs12727104 | 1 | 171454028 | intergenic variant | G/A | snv | 8.3E-02 | 1 | ||||
rs12727980 | 1 | 200289967 | intron variant | C/T | snv | 0.54 | 1 | ||||
rs1276720 | 10 | 16929427 | intron variant | C/T | snv | 0.65 | 1 | ||||
rs13394343 | 2 | 85527219 | intergenic variant | C/A;T | snv | 1 | |||||
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 | |||
rs16943246 | 15 | 45428399 | upstream gene variant | G/A | snv | 0.29 | 1 | ||||
rs17368443 | 11 | 10275289 | intron variant | G/C | snv | 5.3E-02 | 1 | ||||
rs183131780 | 2 | 225820170 | intergenic variant | C/T | snv | 1.0E-03 | 1 | ||||
rs185291443 | 2 | 226120788 | intergenic variant | C/A;G | snv | 1 |