ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.7606G>T (p.Glu2536Ter)

dbSNP: rs886039893
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV000256377 SCV000323173 pathogenic Usher syndrome type 2C no assertion criteria provided clinical testing

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