Related gene-specific medical variations for Gene (Select 2833) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3079205	NM_001504.2(CXCR3):c.972G>C (p.Lys324Asn)	CXCR3, LOC130068420 (K324N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455581	NM_001504.2(CXCR3):c.990G>T (p.Trp330Cys)	CXCR3, LOC130068420 (W330C +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity