ClinVar Miner

Submissions for variant NM_014208.3(DSPP):c.1073G>A (p.Arg358Lys)

gnomAD frequency: 0.00063  dbSNP: rs201110163
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000265736 SCV000345437 uncertain significance not provided 2016-09-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000265736 SCV001043215 likely benign not provided 2024-03-18 criteria provided, single submitter clinical testing
GeneDx RCV000265736 SCV001780299 likely benign not provided 2020-07-31 criteria provided, single submitter clinical testing

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