NM_004530.6(MMP2):c.658+19G>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003661578.1
Allele description [Variation Report for NM_004530.6(MMP2):c.658+19G>A]
NM_004530.6(MMP2):c.658+19G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
LOC102724652 [Homo sapiens]
LOC102724652 [Homo sapiens]Gene ID:102724652Gene
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Last Updated: Feb 28, 2024