Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000020601 | SCV000041089 | not provided | Seizures, benign familial neonatal, 2 | no assertion provided | literature only | ||
OMIM | RCV000020601 | SCV000121584 | pathogenic | Seizures, benign familial neonatal, 2 | 2000-06-01 | no assertion criteria provided | literature only |