ClinVar Miner

Submissions for variant NM_006662.3(SRCAP):c.5610C>T (p.Pro1870=)

gnomAD frequency: 0.00004  dbSNP: rs141985098
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
Eurofins Ntd Llc (ga) RCV000597500 SCV000708810 uncertain significance not provided 2017-06-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000597500 SCV001052647 likely benign not provided 2023-12-18 criteria provided, single submitter clinical testing

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