NM_025193.4(HSD3B7):c.671T>C (p.Val224Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 21, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000595257.4
Allele description [Variation Report for NM_025193.4(HSD3B7):c.671T>C (p.Val224Ala)]
NM_025193.4(HSD3B7):c.671T>C (p.Val224Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024