ClinVar Miner

Submissions for variant NM_001204424.2(RGS6):c.184+7C>T

dbSNP: rs112696041
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000879110 SCV001022122 benign not provided 2024-10-23 criteria provided, single submitter clinical testing
GeneDx RCV000879110 SCV002575627 likely benign not provided 2019-08-16 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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