Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 181 | ||
rs387907272 | 0.572 | 0.520 | 3 | 38141150 | stop lost | T/C | snv | 5.2E-05 | 7.0E-06 | 73 | |
rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 42 | ||
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 23 | |||
rs371769427 | 0.683 | 0.400 | 21 | 43104346 | missense variant | G/A;T | snv | 8.0E-06 | 17 | ||
rs568887534 | 0.807 | 0.240 | 8 | 30183156 | missense variant | A/G | snv | 4.0E-06 | 9 | ||
rs147001633 | 0.776 | 0.240 | 2 | 25234373 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.2E-04 | 9 | ||
rs121913514 | 0.763 | 0.240 | 4 | 54733174 | missense variant | T/A;G | snv | 9 | |||
rs1250394819 | 0.807 | 0.240 | 5 | 115616325 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs1190999960 | 0.807 | 0.240 | 11 | 65571690 | missense variant | G/A | snv | 9 | |||
rs267601394 | 0.807 | 0.200 | 7 | 148811635 | missense variant | T/A;G | snv | 6 | |||
rs373667881 | 0.827 | 0.160 | 8 | 125431222 | missense variant | G/A;T | snv | 1.1E-03 | 5 | ||
rs974120 | 0.851 | 0.200 | 8 | 2789080 | intron variant | T/C;G | snv | 4 | |||
rs9277378 | 0.827 | 0.320 | 6 | 33082502 | intron variant | A/G | snv | 0.40 | 4 | ||
rs397507510 | 0.776 | 0.280 | 12 | 112450361 | missense variant | G/A;C;T | snv | 4 | |||
rs10251201 | 0.851 | 0.160 | 7 | 7932654 | intron variant | T/A;C | snv | 4 | |||
rs377577594 | 0.827 | 0.240 | 2 | 25234374 | missense variant | G/A;C;T | snv | 1.2E-04; 8.0E-06 | 3 | ||
rs9318227 | 0.882 | 0.080 | 13 | 73926833 | intron variant | T/A;C | snv | 3 | |||
rs10405859 | 0.882 | 0.080 | 19 | 45099523 | intron variant | T/C | snv | 0.48 | 3 | ||
rs2239630 | 0.925 | 0.160 | 14 | 23120140 | upstream gene variant | A/C;G | snv | 2 | |||
rs121912472 | 0.925 | 0.080 | 9 | 5073742 | missense variant | G/C | snv | 2 | |||
rs757412228 | 0.925 | 0.080 | 21 | 34886917 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
rs1483790387 | 0.925 | 0.120 | 5 | 115625762 | missense variant | C/A | snv | 2 | |||
rs1217007648 | 1.000 | 0.080 | 8 | 42306376 | missense variant | A/G | snv | 1 |