NM_018662.3(DISC1):c.1816G>C (p.Asp606His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004131370.1
Allele description [Variation Report for NM_018662.3(DISC1):c.1816G>C (p.Asp606His)]
NM_018662.3(DISC1):c.1816G>C (p.Asp606His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
eggc.vipFRl (0)
BioProject
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Last Updated: May 26, 2024