ClinVar Miner

Submissions for variant NM_004568.6(SERPINB6):c.730-32G>A

gnomAD frequency: 0.84542  dbSNP: rs318426
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 RCV001537540 SCV001754433 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807419 SCV002054775 benign Autosomal recessive nonsyndromic hearing loss 91 2021-07-15 criteria provided, single submitter clinical testing

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