NM_000414.4(HSD17B4):c.109G>A (p.Val37Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 27, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000734981.4
Allele description [Variation Report for NM_000414.4(HSD17B4):c.109G>A (p.Val37Ile)]
NM_000414.4(HSD17B4):c.109G>A (p.Val37Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024