ClinVar Miner

Submissions for variant NM_014208.3(DSPP):c.3461_3462insCGATAGCAGCGACAGCAG (p.1152DSS[11])

dbSNP: rs1387872889
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 RCV001598387 SCV001831673 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001598387 SCV004152932 uncertain significance not provided 2023-03-01 criteria provided, single submitter clinical testing DSPP: PM2, BP3

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