ClinVar Miner

Submissions for variant NM_004100.5(EYA4):c.971-7T>C

gnomAD frequency: 0.00007  dbSNP: rs764351261
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000232334 SCV000288094 likely benign Dilated cardiomyopathy 1J 2023-12-06 criteria provided, single submitter clinical testing
GeneDx RCV001582777 SCV001819105 likely benign not provided 2020-12-30 criteria provided, single submitter clinical testing

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