ClinVar Miner

Submissions for variant NM_001371727.1(GABRB2):c.1088A>G (p.Lys363Arg)

dbSNP: rs1561608651
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000688474 SCV000816087 benign Intellectual disability 2019-08-13 criteria provided, single submitter clinical testing

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