ClinVar Miner

Submissions for variant NM_001372106.1(DNAH10):c.11213C>T (p.Thr3738Ile)

gnomAD frequency: 0.00313  dbSNP: rs202063832
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000963103 SCV001110236 likely benign not provided 2018-02-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000963103 SCV004136580 likely benign not provided 2022-12-01 criteria provided, single submitter clinical testing DNAH10: BS2
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000963103 SCV001797782 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001701269 SCV001923170 benign not specified no assertion criteria provided clinical testing

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