Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 484 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913227 | 0.653 | 0.320 | 7 | 140753336 | missense variant | AC/CT;TT | mnv | 31 | |||
rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 23 | ||
rs121913338 | 0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv | 14 | |||
rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 11 | ||
rs1225976306 | 0.807 | 0.160 | 7 | 140924673 | missense variant | C/T | snv | 9.3E-06 | 8 | ||
rs121913366 | 0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv | 7 | |||
rs121913378 | 0.776 | 0.280 | 7 | 140753337 | missense variant | C/A;G;T | snv | 6 | |||
rs121913348 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 5 | |||
rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
rs121913375 | 0.851 | 0.240 | 7 | 140753339 | missense variant | G/A;C | snv | 3 | |||
rs397507482 | 0.882 | 0.040 | 7 | 140753386 | missense variant | A/C | snv | 3 | |||
rs1057519720 | 0.851 | 0.080 | 7 | 140781602 | missense variant | CC/AA;GA | mnv | 2 | |||
rs121913357 | 0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv | 2 | |||
rs121913365 | 0.776 | 0.320 | 7 | 140753332 | missense variant | T/A;G | snv | 2 | |||
rs121913368 | 0.925 | 0.040 | 7 | 140753345 | missense variant | AG/GA | mnv | 2 | |||
rs121913371 | 1.000 | 0.040 | 7 | 140781678 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
rs1057519718 | 0.925 | 0.160 | 7 | 140753355 | missense variant | CA/TC | mnv | 1 | |||
rs121913341 | 0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv | 1 | |||
rs121913376 | 0.925 | 0.080 | 7 | 140781597 | missense variant | C/A;T | snv | 1 | |||
rs1639679 | 1.000 | 0.040 | 7 | 140778454 | intron variant | G/T | snv | 9.8E-02 | 1 | ||
rs397516896 | 0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv | 1 | |||
rs794729219 | 0.882 | 0.240 | 7 | 140753352 | missense variant | A/G | snv | 1 |