Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000010618 | SCV000030844 | pathogenic | Hearing loss, X-linked 1 | 2010-01-01 | no assertion criteria provided | literature only | |
Gene |
RCV000010618 | SCV002599422 | not provided | Hearing loss, X-linked 1 | no assertion provided | literature only |