NM_001289808.2(CRYAB):c.*38G>C AND Myofibrillar myopathy 2
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000282168.5
Allele description [Variation Report for NM_001289808.2(CRYAB):c.*38G>C]
NM_001289808.2(CRYAB):c.*38G>C
Condition(s)
- Name:
- Myofibrillar myopathy 2
- Synonyms:
- MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE; MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED; Alpha-B crystallinopathy; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0012130; MedGen: C1837317; Orphanet: 280553; OMIM: 608810
Assertion and evidence details
Last Updated: Apr 6, 2024