"Department of Medical Genetics, Oslo University Hospital"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 981196	NM_001142784.3(IL11RA):c.281G>T (p.Cys94Phe)	IL11RA (C94F)	Single nucleotide variant (missense variant +1 more)	Craniosynostosis and dental anomalies	GLikely pathogenic
Select item 981195	NM_001142784.3(IL11RA):c.781C>T (p.Arg261Cys)	IL11RA (R261C)	Single nucleotide variant (missense variant +1 more)	Craniosynostosis and dental anomalies	GLikely pathogenic