ClinVar Miner

Submissions for variant NM_001374736.1(DST):c.625+7694C>T

gnomAD frequency: 0.00909  dbSNP: rs1473261823
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001794689 SCV002032589 likely benign not provided 2021-06-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001794689 SCV005222117 likely benign not provided criteria provided, single submitter not provided

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