NM_001174089.2(SLC4A11):c.2018+7A>G AND not provided
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Jun 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000948023.5
Allele description [Variation Report for NM_001174089.2(SLC4A11):c.2018+7A>G]
NM_001174089.2(SLC4A11):c.2018+7A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022