ClinVar Miner

Submissions for variant NM_000742.4(CHRNA2):c.-562GA[8]

dbSNP: rs150699126
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000389425 SCV000473218 uncertain significance Sleep-related hypermotor epilepsy 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003437139 SCV004164545 benign not provided 2022-10-01 criteria provided, single submitter clinical testing CHRNA2: BS1, BS2

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