NM_020442.6(VARS2):c.2328C>T (p.Ser776=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000435108.1
Allele description [Variation Report for NM_020442.6(VARS2):c.2328C>T (p.Ser776=)]
NM_020442.6(VARS2):c.2328C>T (p.Ser776=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024