ClinVar Miner

Submissions for variant NM_005982.4(SIX1):c.*265del

dbSNP: rs112733948
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000402316 SCV000387278 benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000297057 SCV000387279 benign Branchiootorenal Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001613001 SCV001835359 benign not provided 2019-08-10 criteria provided, single submitter clinical testing

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