NM_001848.3(COL6A1):c.428+39C>G AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Sep 5, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000079812.13
Allele description [Variation Report for NM_001848.3(COL6A1):c.428+39C>G]
NM_001848.3(COL6A1):c.428+39C>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Sep 29, 2024