NM_000190.4(HMBS):c.772-7G>C AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002158871.6
Allele description [Variation Report for NM_000190.4(HMBS):c.772-7G>C]
NM_000190.4(HMBS):c.772-7G>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024