ClinVar Miner

Submissions for variant NM_006846.4(SPINK5):c.666+10C>T

gnomAD frequency: 0.00001  dbSNP: rs773205014
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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 RCV001452888 SCV001656565 likely benign Netherton syndrome 2018-11-13 criteria provided, single submitter clinical testing

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