Related gene-specific medical variations for Gene (Select 126859963) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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)	not provided +1 more	GBenign
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 14718	NC_000007.14:g.22727026C>G	IL6-AS1, LOC126859963 +1 more	Single nucleotide variant (genic upstream transcript variant)	Diabetes mellitus type 2, susceptibility to +5 more	Gother; risk factor

ClinVar