ClinVar Miner

Submissions for variant NM_015375.3(DSTYK):c.2105+10G>A

gnomAD frequency: 0.00131  dbSNP: rs200576489
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002088222 SCV002377173 benign not provided 2024-08-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002088222 SCV005281765 benign not provided criteria provided, single submitter not provided

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