ClinVar Miner

Submissions for variant NM_016277.5(RAB23):c.576T>G (p.Gly192=)

dbSNP: rs2127996390
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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 RCV002203956 SCV002487243 likely benign Carpenter syndrome 2021-01-11 criteria provided, single submitter clinical testing

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