NM_000257.4(MYH7):c.-9+23T>C AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 23, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001658798.9
Allele description [Variation Report for NM_000257.4(MYH7):c.-9+23T>C]
NM_000257.4(MYH7):c.-9+23T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Jun 2, 2024