ClinVar Miner

Submissions for variant NM_001388453.1(QRICH2):c.4748+47G>A

gnomAD frequency: 0.41462  dbSNP: rs164010
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001794867 SCV002033378 benign Spermatogenic failure 35 2021-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710374 SCV005252401 benign not provided criteria provided, single submitter not provided

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