NM_001077365.2(POMT1):c.1826-40G>A AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Feb 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243493.9
Allele description [Variation Report for NM_001077365.2(POMT1):c.1826-40G>A]
NM_001077365.2(POMT1):c.1826-40G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024