ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.*4113dup

dbSNP: rs138193115
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000353519 SCV000465532 likely benign Nonsyndromic Hearing Loss, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000260999 SCV000465533 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001718770 SCV001948862 benign not provided 2021-05-13 criteria provided, single submitter clinical testing

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