ClinVar Miner

Submissions for variant NM_001374736.1(DST):c.3186+87G>A

gnomAD frequency: 0.00852  dbSNP: rs150155934
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001733086 SCV001983250 likely benign not provided 2021-04-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001733086 SCV005222113 likely benign not provided criteria provided, single submitter not provided

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