ClinVar Miner

Submissions for variant NM_002872.5(RAC2):c.12C>T (p.Ile4=)

dbSNP: rs996009169
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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 RCV001447998 SCV001651078 likely benign Neutrophil immunodeficiency syndrome 2018-11-30 criteria provided, single submitter clinical testing

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