ClinVar Miner

Submissions for variant NM_025193.4(HSD3B7):c.103C>G (p.Arg35Gly)

gnomAD frequency: 0.00282  dbSNP: rs150464212
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000175950 SCV000227528 benign not specified 2014-11-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000882053 SCV001025270 benign not provided 2024-01-06 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000882053 SCV004227560 uncertain significance not provided 2023-01-09 criteria provided, single submitter clinical testing BS1
CeGaT Center for Human Genetics Tuebingen RCV000882053 SCV005051292 likely benign not provided 2024-05-01 criteria provided, single submitter clinical testing HSD3B7: BS1

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