NM_001006607.3(LRRC37A2):c.3537C>G (p.Phe1179Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004415474.1
Allele description [Variation Report for NM_001006607.3(LRRC37A2):c.3537C>G (p.Phe1179Leu)]
NM_001006607.3(LRRC37A2):c.3537C>G (p.Phe1179Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024