ClinVar Miner

Submissions for variant NM_020717.5(SHROOM4):c.3414delinsGGAG (p.Glu1151dup)

dbSNP: rs886044870
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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) RCV000322654 SCV000341253 benign not specified 2016-04-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494870 SCV002802829 likely benign X-linked intellectual disability, Stocco dos Santos type 2021-11-18 criteria provided, single submitter clinical testing

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