NM_025193.4(HSD3B7):c.637G>A (p.Gly213Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004020149.1
Allele description [Variation Report for NM_025193.4(HSD3B7):c.637G>A (p.Gly213Arg)]
NM_025193.4(HSD3B7):c.637G>A (p.Gly213Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
ZNF461 zinc finger protein 461 [Homo sapiens]
ZNF461 zinc finger protein 461 [Homo sapiens]Gene ID:92283Gene
-
Gene Links for GEO Profiles (Select 128529946) (1)
Gene
-
LINC00665 long intergenic non-protein coding RNA 665 [Homo sapiens]
LINC00665 long intergenic non-protein coding RNA 665 [Homo sapiens]Gene ID:100506930Gene
-
Gene Links for GEO Profiles (Select 128491702) (1)
Gene
-
ZNF382 zinc finger protein 382 [Homo sapiens]
ZNF382 zinc finger protein 382 [Homo sapiens]Gene ID:84911Gene
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Last Updated: Sep 29, 2024