NM_000237.3(LPL):c.456T>C (p.Asn152=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002336874.4
Allele description [Variation Report for NM_000237.3(LPL):c.456T>C (p.Asn152=)]
NM_000237.3(LPL):c.456T>C (p.Asn152=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
-
Homo sapiens cDNA, FLJ18072
Homo sapiens cDNA, FLJ18072gi|164694606|dbj|AK311030.1|Nucleotide
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Last Updated: May 1, 2024