ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.1241+40C>G

gnomAD frequency: 0.05050  dbSNP: rs59360049
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 RCV001539329 SCV001757088 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001539329 SCV005299457 benign not provided criteria provided, single submitter not provided

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