ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.17794A>C (p.Arg5932=)

gnomAD frequency: 0.00001  dbSNP: rs747728554
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000594070 SCV000707291 uncertain significance not provided 2017-04-04 criteria provided, single submitter clinical testing
Invitae RCV000594070 SCV004397427 likely benign not provided 2023-03-09 criteria provided, single submitter clinical testing

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