NM_012156.2(EPB41L1):c.566+7G>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 20, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000933837.3
Allele description [Variation Report for NM_012156.2(EPB41L1):c.566+7G>A]
NM_012156.2(EPB41L1):c.566+7G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022