Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs111401431 | 0.763 | 0.200 | 15 | 48468097 | missense variant | G/A | snv | 2 | |||
rs137854459 | 1.000 | 0.160 | 15 | 48463977 | missense variant | A/G | snv | 1 | |||
rs111929350 | 1.000 | 0.160 | 15 | 48452603 | missense variant | C/A;G;T | snv | 1 | |||
rs112728248 | 0.925 | 0.160 | 15 | 48448812 | missense variant | C/T | snv | 1 | |||
rs363804 | 1.000 | 0.160 | 15 | 48441771 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs363815 | 1.000 | 0.160 | 15 | 48437370 | missense variant | A/G | snv | 1 | |||
rs137854461 | 0.790 | 0.280 | 15 | 48437026 | missense variant | T/C | snv | 1 | |||
rs137854460 | 0.925 | 0.160 | 15 | 48432943 | missense variant | C/G;T | snv | 1 | |||
rs112836174 | 0.925 | 0.160 | 15 | 48430791 | missense variant | A/G;T | snv | 1 | |||
rs137854457 | 0.925 | 0.160 | 15 | 48428423 | missense variant | C/G;T | snv | 1 | |||
rs111588631 | 1.000 | 0.160 | 15 | 48428391 | missense variant | A/G | snv | 1 | |||
rs137854464 | 0.851 | 0.200 | 15 | 48425483 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs113544411 | 0.925 | 0.160 | 15 | 48421652 | stop gained | G/A;C;T | snv | 1.2E-05 | 1 | ||
rs111984349 | 0.763 | 0.200 | 15 | 48415759 | missense variant | C/T | snv | 1 | |||
rs141133182 | 1.000 | 0.160 | 15 | 48415735 | stop gained | C/A;T | snv | 2.1E-04 | 1 |