NM_213599.3(ANO5):c.2521-13A>G AND not specified
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Jan 12, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000082847.15
Allele description [Variation Report for NM_213599.3(ANO5):c.2521-13A>G]
NM_213599.3(ANO5):c.2521-13A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024