NM_013296.5(GPSM2):c.1063-1G>T AND Rare genetic deafness
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Sep 17, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000218080.4
Allele description [Variation Report for NM_013296.5(GPSM2):c.1063-1G>T]
NM_013296.5(GPSM2):c.1063-1G>T
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024