ClinVar Miner

Submissions for variant NM_004568.6(SERPINB6):c.573+26A>G

gnomAD frequency: 0.63676  dbSNP: rs2244693
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001645148 SCV001855303 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807457 SCV002054776 benign Autosomal recessive nonsyndromic hearing loss 91 2021-07-15 criteria provided, single submitter clinical testing

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