NM_004839.4(HOMER2):c.387+6A>T AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000611167.1
Allele description [Variation Report for NM_004839.4(HOMER2):c.387+6A>T]
NM_004839.4(HOMER2):c.387+6A>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024