ClinVar Miner

Submissions for variant NM_000431.4(MVK):c.79-164T>G

gnomAD frequency: 0.55050  dbSNP: rs6606734
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000507457 SCV000604312 benign not specified 2018-07-03 criteria provided, single submitter clinical testing
GeneDx RCV001675912 SCV001894427 benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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