Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 4 | ||
rs11814448 | 0.925 | 0.080 | 10 | 22026914 | intergenic variant | A/C | snv | 0.21 | 1 | ||
rs3734805 | 0.925 | 0.080 | 6 | 151618215 | 3 prime UTR variant | A/C | snv | 6.9E-02 | 1 | ||
rs6180 | 0.827 | 0.160 | 5 | 42719137 | missense variant | A/C | snv | 0.44 | 0.43 | 1 | |
rs6815814 | 1.000 | 0.080 | 4 | 38814717 | intron variant | A/C | snv | 0.43 | 1 | ||
rs9693444 | 0.925 | 0.080 | 8 | 29652100 | intergenic variant | A/C | snv | 0.66 | 1 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 2 | |||
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 2 | ||
rs7107217 | 0.882 | 0.160 | 11 | 129603795 | intron variant | A/C;G | snv | 2 | |||
rs11196174 | 1.000 | 0.080 | 10 | 112974337 | intron variant | A/C;G | snv | 1 | |||
rs17879961 | 0.597 | 0.480 | 22 | 28725099 | missense variant | A/C;G | snv | 4.1E-03 | 1 | ||
rs2543519 | 0.925 | 0.080 | 22 | 37084229 | missense variant | A/C;G | snv | 0.22 | 1 | ||
rs12906542 | 0.925 | 0.080 | 15 | 77977130 | intron variant | A/C;G;T | snv | 1 | |||
rs1447295 | 0.658 | 0.400 | 8 | 127472793 | intron variant | A/C;T | snv | 2 | |||
rs1316170 | 1.000 | 0.080 | 14 | 68231755 | intron variant | A/C;T | snv | 1 | |||
rs2228468 | 0.882 | 0.120 | 3 | 42865620 | missense variant | A/C;T | snv | 0.43; 8.3E-03 | 1 | ||
rs6913578 | 0.925 | 0.080 | 6 | 151628671 | intergenic variant | A/C;T | snv | 1 | |||
rs7716600 | 0.925 | 0.080 | 5 | 44874903 | regulatory region variant | A/C;T | snv | 1 | |||
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 5 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 4 | ||
rs10811650 | 0.882 | 0.200 | 9 | 22067594 | intron variant | A/G | snv | 0.37 | 4 | ||
rs9257809 | 0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 | 4 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 3 | ||
rs3803662 | 0.662 | 0.440 | 16 | 52552429 | non coding transcript exon variant | A/G | snv | 0.63 | 3 |