NM_001038603.3(MARVELD2):c.197C>G (p.Thr66Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002826736.2
Allele description [Variation Report for NM_001038603.3(MARVELD2):c.197C>G (p.Thr66Arg)]
NM_001038603.3(MARVELD2):c.197C>G (p.Thr66Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Neoplasm of uterus
Neoplasm of uterusMedGen
-
C0042138[conceptid] (1)
MedGen
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Last Updated: May 1, 2024