ClinVar Miner

Submissions for variant NM_002473.5(MYH9):c.-182G>T

gnomAD frequency: 0.00179  dbSNP: rs868824019
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000271148 SCV000438506 uncertain significance MYH9-related disorder 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000321606 SCV000438507 uncertain significance Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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