ClinVar for MedGen (Select 401085) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1802614	NM_001569.4(IRAK1):c.1138C>T (p.Arg380Trp)	IRAK1 (R380W +1 more)	Single nucleotide variant (missense variant)	Inguinal hernia +5 more	GUncertain significance
Select item 268023	46;X;t(X;21)(q26.1;q21.22)dn		Translocation	Delayed speech and language development +15 more	GUncertain significance