ClinVar Miner

Submissions for variant NM_025193.4(HSD3B7):c.234C>T (p.Ala78=)

gnomAD frequency: 0.00104  dbSNP: rs143699328
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000592183 SCV000703274 uncertain significance not provided 2018-06-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000592183 SCV001120243 benign not provided 2024-12-04 criteria provided, single submitter clinical testing

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