Lissencephaly Type 1 Due to Doublecortin Gene Mutation
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Associated Genes (1)
Associated Variants (39)
| RSID | Gene | Evidence |
|---|---|---|
| RS1921404698 | DCX | strong |
| RS587783519 | DCX | strong |
| RS797045512 | DCX | strong |
| RS1064794223 | DCX | strong |
| RS1556401744 | DCX | strong |
| RS1556401951 | DCX | strong |
| RS1556405129 | DCX | strong |
| RS761786389 | DCX | strong |
| RS1603423268 | DCX | strong |
| RS1921403332 | DCX | strong |
| RS587783534 | DCX | strong |
| RS2147263208 | DCX | strong |
| RS2147262801 | DCX | strong |
| RS2147263018 | DCX | strong |
| RS2524858685 | DCX | strong |
| RS2524859237 | DCX | strong |
| RS2524858642 | DCX | strong |
| RS2524627990 | DCX | strong |
| RS2524835526 | DCX | strong |
| RS2524628032 | DCX | strong |
| RS587783590 | DCX | strong |
| RS104894780 | DCX | strong |
| RS104894781 | DCX | strong |
| RS122457137 | DCX | strong |
| RS104894782 | DCX | strong |
| RS104894784 | DCX | strong |
| RS56030372 | DCX | strong |
| RS104894786 | DCX | strong |
| RS267606317 | DCX | strong |
| RS587783592 | DCX | strong |
| RS104894779 | DCX | strong |
| RS587783589 | DCX | strong |
| RS587783577 | DCX | strong |
| RS587783568 | DCX | strong |
| RS587783563 | DCX | strong |
| RS587783559 | DCX | strong |
| RS587783558 | DCX | strong |
| RS587783541 | DCX | strong |
| RS61729440 | DCX | strong |