ClinVar Miner

Submissions for variant NM_004218.4(RAB11B):c.40+15G>T

dbSNP: rs777551842
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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 RCV002159677 SCV002337335 likely benign not provided 2021-08-19 criteria provided, single submitter clinical testing

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