ClinVar Miner

Submissions for variant NM_006846.4(SPINK5):c.2667-13_2667-12insTT

gnomAD frequency: 0.00001  dbSNP: rs1561704956
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002216780 SCV002367535 likely benign Netherton syndrome 2021-04-05 criteria provided, single submitter clinical testing

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