ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.209G>A (p.Gly70Asp)

dbSNP: rs1559996059
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV000735691 SCV000863838 uncertain significance Usher syndrome type 3 2018-03-22 no assertion criteria provided clinical testing

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