NM_000553.6(WRN):c.505-4C>G AND Werner syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000633297.9
Allele description [Variation Report for NM_000553.6(WRN):c.505-4C>G]
NM_000553.6(WRN):c.505-4C>G
Condition(s)
-
LOC102724874 [Homo sapiens]
LOC102724874 [Homo sapiens]Gene ID:102724874Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024