NM_000543.5(SMPD1):c.996C>G (p.Pro332=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001501214.9
Allele description [Variation Report for NM_000543.5(SMPD1):c.996C>G (p.Pro332=)]
NM_000543.5(SMPD1):c.996C>G (p.Pro332=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024