ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1925-30G>A

gnomAD frequency: 0.00641  dbSNP: rs149916101
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241686 SCV000314921 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001753730 SCV002006727 likely benign not provided 2019-06-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001753730 SCV005215154 likely benign not provided criteria provided, single submitter not provided
Leiden Open Variation Database RCV000241686 SCV001364724 likely benign not specified 2012-08-31 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Janine Bakker.

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