ClinVar Miner

Submissions for variant NM_014208.3(DSPP):c.3274A>G (p.Asn1092Asp)

gnomAD frequency: 0.75295  dbSNP: rs201754564
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
GeneDx RCV001613789 SCV001834611 benign not provided 2018-11-10 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 30245029, 27884173, 25342930)
Breakthrough Genomics, Breakthrough Genomics RCV001613789 SCV005303254 benign not provided criteria provided, single submitter not provided

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