ClinVar Miner

Submissions for variant NM_138615.3(DHX30):c.2930-4C>T

gnomAD frequency: 0.00005  dbSNP: rs537095382
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 RCV000883621 SCV001026943 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000883621 SCV001875276 likely benign not provided 2021-03-05 criteria provided, single submitter clinical testing

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