"GenomeConnect, ClinGen"[submitter] AND "IL1RAPL1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 421811	NM_014271.4(IL1RAPL1):c.621AGA[1] (p.Glu208del)	IL1RAPL1 (E208del)	Microsatellite (inframe_deletion)	not provided	GLikely pathogenic
Select item 1339877	GRCh37/hg19 Xp21.2(chrX:29417558-29938361)x3	IL1RAPL1	Copy number gain	not provided	Gnot provided
Select item 684515	Single allele	DCAF8L1, DCAF8L2 +12 more	Deletion	Chromosome Xp21 deletion syndrome	Gnot provided

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