ClinVar Miner

Submissions for variant NM_001543.5(NDST1):c.1970+10C>T

gnomAD frequency: 0.00697  dbSNP: rs75978931
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514842 SCV000610303 likely benign not provided 2017-06-15 criteria provided, single submitter clinical testing
Invitae RCV000514842 SCV001055515 benign not provided 2024-01-01 criteria provided, single submitter clinical testing

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