ClinVar Miner

Submissions for variant NM_005506.4(SCARB2):c.1399-206A>G

gnomAD frequency: 0.00344  dbSNP: rs60271776
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001551232 SCV001771696 likely benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001551232 SCV005257903 likely benign not provided criteria provided, single submitter not provided

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