ClinVar Miner

Submissions for variant NM_000964.4(RARA):c.827G>A (p.Arg276Gln)

dbSNP: rs2034543510
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001266577 SCV001444753 likely pathogenic Inborn genetic diseases 2016-09-28 criteria provided, single submitter clinical testing
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV002221619 SCV002499083 uncertain significance not provided 2022-03-01 criteria provided, single submitter clinical testing Gene of Uncertain Clinical Significance

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