ClinVar Miner

Submissions for variant NM_021116.4(ADCY1):c.1149-31C>G

gnomAD frequency: 0.70197  dbSNP: rs2461131
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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 RCV001549071 SCV001769150 benign Autosomal recessive nonsyndromic hearing loss 44 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001676053 SCV001895679 benign not provided 2018-11-10 criteria provided, single submitter clinical testing

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