ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.14928C>T (p.His4976=)

dbSNP: rs1251473317
Minimum review status: Collection method:
Minimum conflict level:
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) RCV000728065 SCV000855591 uncertain significance not provided 2017-07-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000728065 SCV002973700 likely benign not provided 2024-02-14 criteria provided, single submitter clinical testing

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