NM_175940.3(DUOX1):c.1733C>T (p.Ala578Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002906570.1
Allele description
NM_175940.3(DUOX1):c.1733C>T (p.Ala578Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Erectile dysfunction
Erectile dysfunctionMedGen
-
C0242350[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Feb 13, 2023