ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.14943G>C (p.Gln4981His) (rs200153555)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000155117 SCV000204803 benign not specified 2012-04-30 criteria provided, single submitter clinical testing Gln4981His in Exon 73 of GPR98: This variant is not expected to have clinical si gnificance because it has been identified in 0.7% (20/3016) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http: //
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000155117 SCV000340139 likely benign not specified 2016-04-04 criteria provided, single submitter clinical testing
Invitae RCV000968059 SCV001115489 likely benign not provided 2020-12-04 criteria provided, single submitter clinical testing

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