NM_000145.4(FSHR):c.668+268T>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001548523.2
Allele description [Variation Report for NM_000145.4(FSHR):c.668+268T>G]
NM_000145.4(FSHR):c.668+268T>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023