NM_001083961.2(WDR62):c.4187G>A (p.Arg1396His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 11, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000193946.7
Allele description [Variation Report for NM_001083961.2(WDR62):c.4187G>A (p.Arg1396His)]
NM_001083961.2(WDR62):c.4187G>A (p.Arg1396His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 23, 2024