Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 4 | ||
rs121913341 | 0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv | 2 | |||
rs121913351 | 0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 | 2 | ||
rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 2 | ||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
rs121913338 | 0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv | 1 | |||
rs121913348 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 1 | |||
rs121913357 | 0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv | 1 | |||
rs121913361 | 0.807 | 0.280 | 7 | 140753349 | missense variant | C/A;G;T | snv | 1 | |||
rs121913366 | 0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv | 1 | |||
rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs121913370 | 0.763 | 0.360 | 7 | 140753393 | missense variant | T/C;G | snv | 1 | |||
rs121913375 | 0.851 | 0.240 | 7 | 140753339 | missense variant | G/A;C | snv | 1 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
rs104894094 | 0.763 | 0.200 | 9 | 21971058 | missense variant | C/A;G;T | snv | 8.5E-06; 4.3E-06 | 2 | ||
rs1064794292 | 0.882 | 0.200 | 9 | 21974760 | missense variant | C/T | snv | 2 | |||
rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 1 | ||
rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 1 | ||
rs104894098 | 0.851 | 0.200 | 9 | 21970982 | missense variant | A/T | snv | 1 | |||
rs104894099 | 0.851 | 0.200 | 9 | 21971183 | missense variant | A/C;T | snv | 4.6E-06 | 1 | ||
rs121913386 | 0.807 | 0.120 | 9 | 21971018 | missense variant | G/A;T | snv | 1 | |||
rs137854599 | 0.882 | 0.080 | 9 | 21971093 | missense variant | C/G;T | snv | 1 | |||
rs1554653960 | 0.925 | 0.040 | 9 | 21971007 | missense variant | C/T | snv | 1 | |||
rs36204594 | 1.000 | 0.040 | 9 | 21971180 | missense variant | G/A;T | snv | 1 | |||
rs758389471 | 0.882 | 0.080 | 9 | 21971160 | missense variant | C/G;T | snv | 4.7E-06; 4.7E-06 | 1 |