NM_001164508.2(NEB):c.23013C>T (p.Ser7671=) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000724373.29
Allele description [Variation Report for NM_001164508.2(NEB):c.23013C>T (p.Ser7671=)]
NM_001164508.2(NEB):c.23013C>T (p.Ser7671=)
Condition(s)
- Synonyms:
- none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jan 19, 2025