NM_207361.6(FREM2):c.1345C>G (p.Leu449Val) AND Fraser syndrome 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001113632.4
Allele description [Variation Report for NM_207361.6(FREM2):c.1345C>G (p.Leu449Val)]
NM_207361.6(FREM2):c.1345C>G (p.Leu449Val)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024