NM_080732.4(EGLN2):c.28C>T (p.Leu10=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004063097.1
Allele description [Variation Report for NM_080732.4(EGLN2):c.28C>T (p.Leu10=)]
NM_080732.4(EGLN2):c.28C>T (p.Leu10=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Oct 8, 2024