ClinVar Miner

Submissions for variant NM_018136.5(ASPM):c.8309T>G (p.Val2770Gly)

dbSNP: rs886043529
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000725923 SCV000340547 uncertain significance not provided 2016-03-31 criteria provided, single submitter clinical testing
GeneDx RCV000725923 SCV000535925 likely benign not provided 2019-08-22 criteria provided, single submitter clinical testing

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