ClinVar Miner

Submissions for variant NM_003922.4(HERC1):c.13808T>C (p.Leu4603Pro)

dbSNP: rs2152730050
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001822309 SCV002066435 uncertain significance not specified 2017-07-28 criteria provided, single submitter clinical testing

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