ClinVar Miner

Submissions for variant NM_201599.3(ZMYM3):c.195C>G (p.Gly65=)

gnomAD frequency: 0.00102  dbSNP: rs139405380
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000154163 SCV000203829 uncertain significance not provided 2013-12-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000154163 SCV001079720 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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