ClinVar Miner

Submissions for variant NM_001005373.4(LRSAM1):c.904-48G>A

gnomAD frequency: 0.00802  dbSNP: rs143901401
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001559635 SCV001781907 likely benign not provided 2019-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001559635 SCV005227496 likely benign not provided criteria provided, single submitter not provided

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