NM_024592.5(SRD5A3):c.124G>A (p.Gly42Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002559449.2
Allele description [Variation Report for NM_024592.5(SRD5A3):c.124G>A (p.Gly42Ser)]
NM_024592.5(SRD5A3):c.124G>A (p.Gly42Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
GPD2 [Papio anubis]
GPD2 [Papio anubis]Gene ID:101002517Gene
-
HS3ST6 [Papio anubis]
HS3ST6 [Papio anubis]Gene ID:101020207Gene
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Last Updated: May 1, 2024