ClinVar Miner

Submissions for variant NM_181332.3(NLGN4X):c.1254_1255del (p.Glu418fs)

dbSNP: rs1569118680
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV002470708 SCV000032031 pathogenic X-linked intellectual disability 2004-03-01 no assertion criteria provided literature only
OMIM RCV000032596 SCV000056347 risk factor Autism, susceptibility to, X-linked 2 2004-03-01 no assertion criteria provided literature only

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