NM_001257291.2(SLC9A7):c.1032G>C (p.Val344=) AND SLC9A7-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003921794.1
Allele description [Variation Report for NM_001257291.2(SLC9A7):c.1032G>C (p.Val344=)]
NM_001257291.2(SLC9A7):c.1032G>C (p.Val344=)
Condition(s)
- Name:
- SLC9A7-related disorder
- Synonyms:
- SLC9A7-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024