ClinVar Miner

Submissions for variant NM_000780.4(CYP7A1):c.297A>G (p.Lys99=)

gnomAD frequency: 0.00014  dbSNP: rs184906718
Minimum review status: Collection method:
Minimum conflict level:
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) RCV000598516 SCV000701721 likely benign not specified 2016-09-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002062001 SCV002431124 benign not provided 2024-01-20 criteria provided, single submitter clinical testing

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