"Ambry Genetics"[submitter] AND "IL6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2245276	NM_000600.5(IL6):c.119C>A (p.Ala40Asp)	IL6, IL6-AS1 +1 more (A17D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495660	NM_000600.5(IL6):c.168A>C (p.Gln56His)	IL6, IL6-AS1 +1 more (Q33H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2406494	NM_000600.5(IL6):c.285G>C (p.Met95Ile)	IL6 (M19I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285905	NM_000600.5(IL6):c.326A>G (p.Glu109Gly)	IL6 (E86G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534860	NM_000600.5(IL6):c.549C>A (p.Asn183Lys)	IL6 (N160K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303034	NM_000600.5(IL6):c.620G>C (p.Arg207Thr)	IL6 (R184T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar