NM_207361.6(FREM2):c.7873C>A (p.Arg2625Ser) 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:
- RCV001114099.4
Allele description [Variation Report for NM_207361.6(FREM2):c.7873C>A (p.Arg2625Ser)]
NM_207361.6(FREM2):c.7873C>A (p.Arg2625Ser)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024