ClinVar Miner

Submissions for variant NM_014140.4(SMARCAL1):c.863-39C>G

dbSNP: rs73988775
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 RCV001654521 SCV001867995 benign not provided 2021-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001654521 SCV005243947 benign not provided criteria provided, single submitter not provided

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