CXCL6[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270408	NM_002993.4(CXCL6):c.181A>G (p.Lys61Glu)	CXCL6 (K61E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217943	NM_002993.4(CXCL6):c.182A>G (p.Lys61Arg)	CXCL6 (K61R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079185	NM_002993.4(CXCL6):c.223T>C (p.Cys75Arg)	CXCL6 (C75R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710320	NM_002993.4(CXCL6):c.239dup (p.Val81fs)	CXCL6 (V81fs)	Duplication (frameshift variant)	not provided	GBenign
Select item 2558188	NM_002993.4(CXCL6):c.239T>G (p.Val80Gly)	CXCL6 (V80G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231198	NM_002993.4(CXCL6):c.295C>G (p.Leu99Val)	CXCL6 (L99V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270407	NM_002993.4(CXCL6):c.340A>G (p.Asn114Asp)	CXCL6 (N114D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar