NM_000238.4(KCNH2):c.1129-18C>A AND Long QT syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003649110.1
Allele description [Variation Report for NM_000238.4(KCNH2):c.1129-18C>A]
NM_000238.4(KCNH2):c.1129-18C>A
Condition(s)
- Name:
- Long QT syndrome (LQTS)
- Identifiers:
- MONDO: MONDO:0002442; MeSH: D008133; MedGen: C0023976
-
Homo sapiens phosphodiesterase 9A (PDE9A), transcript variant 4, mRNA
Homo sapiens phosphodiesterase 9A (PDE9A), transcript variant 4, mRNAgi|1890269338|ref|NM_001001569.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024