ClinVar Miner

Submissions for variant NM_144498.4(OSBPL2):c.37+23G>A

gnomAD frequency: 0.85800  dbSNP: rs6089706
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001715645 SCV001942904 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788824 SCV002029317 benign Autosomal dominant nonsyndromic hearing loss 67 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001715645 SCV005308221 benign not provided criteria provided, single submitter not provided

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