NM_001038603.3(MARVELD2):c.900G>A (p.Leu300=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Oct 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000151015.6
Allele description [Variation Report for NM_001038603.3(MARVELD2):c.900G>A (p.Leu300=)]
NM_001038603.3(MARVELD2):c.900G>A (p.Leu300=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024