ClinVar Miner

Submissions for variant NM_016277.5(RAB23):c.234C>T (p.Tyr78=)

dbSNP: rs2128002860
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001466121 SCV001670120 likely benign Carpenter syndrome 2020-10-30 criteria provided, single submitter clinical testing

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