"Invitae"[submitter] AND "IL6-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 709119	NM_000600.5(IL6):c.91C>A (p.Pro31Thr)	IL6, IL6-AS1 +1 more (P31T +1 more)	Single nucleotide variant (missense variant +1 more)	IL6-related condition +1 more	GBenign
Select item 768143	NM_000600.5(IL6):c.94C>T (p.Pro32Ser)	IL6, IL6-AS1 +1 more (P32S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 717506	NM_000600.5(IL6):c.183C>T (p.Leu61=)	IL6, IL6-AS1 +1 more	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 708101	NM_000600.5(IL6):c.195A>C (p.Ser65=)	IL6, IL6-AS1 +1 more	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2424085	NC_000007.13:g.(?_20994491)_(23030730_?)del	CDCA7L, DNAH11 +7 more	Deletion	Hypomyelination and Congenital Cataract +1 more	GPathogenic
Select item 1410399	NC_000007.13:g.(?_20994491)_(23213917_?)dup	CDCA7L, DNAH11 +9 more	Duplication	Primary ciliary dyskinesia	GUncertain significance

ClinVar