Related gene-specific medical variations for Gene (Select 6372) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3079186	NM_002993.4(CXCL6):c.86C>T (p.Thr29Met)	CXCL6, LOC123477759 (T29M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252680	NM_002993.4(CXCL6):c.32T>C (p.Val11Ala)	CXCL6, LOC123477759 (V11A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248884	NM_002993.4(CXCL6):c.62T>A (p.Leu21Gln)	CXCL6, LOC123477759 (L21Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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