Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3805382 | 4 | 55605384 | intron variant | A/G | snv | 0.36 | 0.29 | 1 | |||
rs10995311 | 10 | 62805174 | missense variant | C/G | snv | 0.35 | 0.31 | 3 | |||
rs35572189 | 17 | 81451999 | missense variant | G/A;C | snv | 0.34 | 1 | ||||
rs2236295 | 10 | 62805132 | missense variant | G/C;T | snv | 0.32 | 2 | ||||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs1801239 | 0.827 | 0.160 | 10 | 16877053 | missense variant | T/C;G | snv | 8.9E-02; 8.0E-06 | 1 | ||
rs45551835 | 1.000 | 0.080 | 10 | 16890385 | missense variant | G/A;T | snv | 1.3E-02; 4.0E-06 | 2 | ||
rs144360241 | 10 | 16925418 | missense variant | T/C | snv | 5.6E-03 | 5.3E-03 | 1 | |||
rs141640975 | 10 | 16950012 | missense variant | G/A | snv | 1.7E-03 | 1.5E-03 | 1 | |||
rs144994089 | 9 | 33385158 | missense variant | C/T | snv | 7.0E-04 | 8.2E-04 | 1 | |||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 8 | ||||
rs2472297 | 0.882 | 0.160 | 15 | 74735539 | intergenic variant | C/T | snv | 0.16 | 5 | ||
rs4410790 | 0.882 | 0.160 | 7 | 17244953 | intron variant | T/C | snv | 0.54 | 5 | ||
rs2470893 | 0.882 | 0.160 | 15 | 74727108 | upstream gene variant | C/T | snv | 0.20 | 4 | ||
rs784257 | 1.000 | 0.080 | 18 | 55729968 | intron variant | T/A;C | snv | 4 | |||
rs702634 | 1.000 | 0.080 | 5 | 53975590 | intron variant | G/A | snv | 0.72 | 3 | ||
rs112607182 | 3 | 170309619 | downstream gene variant | C/T | snv | 5.3E-02 | 2 | ||||
rs146311723 | 1.000 | 0.080 | 15 | 63512308 | intron variant | T/C | snv | 0.14 | 2 | ||
rs17158386 | 7 | 29765745 | regulatory region variant | G/A | snv | 0.19 | 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 |