ClinVar Miner

Submissions for variant NC_000014.9:g.35405648T>C

gnomAD frequency: 0.26291  dbSNP: rs3138053
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001517841 SCV001726426 benign Ectodermal dysplasia and immunodeficiency 2 2025-02-03 criteria provided, single submitter clinical testing

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