NM_005654.6(NR2F1):c.-1761A>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002281245.2
Allele description [Variation Report for NM_005654.6(NR2F1):c.-1761A>G]
NM_005654.6(NR2F1):c.-1761A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Oct 14, 2023