NM_001159699.2(FHL1):c.502A>T (p.Thr168Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003145628.3
Allele description [Variation Report for NM_001159699.2(FHL1):c.502A>T (p.Thr168Ser)]
NM_001159699.2(FHL1):c.502A>T (p.Thr168Ser)
Condition(s)
- Synonyms:
- none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jan 13, 2025