ClinVar Miner

Submissions for variant NM_001292063.2(OTOG):c.6197A>G (p.His2066Arg)

dbSNP: rs770170338
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001333069 SCV001525554 uncertain significance Autosomal recessive nonsyndromic hearing loss 18B 2019-09-11 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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