ClinVar Miner

Submissions for variant NM_007375.4(TARDBP):c.714+69dup

dbSNP: rs143130606
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000625046 SCV000743619 benign Amyotrophic lateral sclerosis type 10 2016-06-06 criteria provided, single submitter clinical testing
GeneDx RCV001692234 SCV001906869 benign not provided 2018-12-24 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000625046 SCV000745749 benign Amyotrophic lateral sclerosis type 10 2015-04-21 no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579709 SCV001808205 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001579709 SCV001927589 benign not specified no assertion criteria provided clinical testing

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