"PreventionGenetics, part of Exact Sciences"[submitter] AND "CCR2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8267	NM_001123396.4(CCR2):c.190G>A (p.Val64Ile)	CCR2 (V64I)	Single nucleotide variant (missense variant)	CCR2-related disorder	GBenign
Select item 3042378	NM_001123396.4(CCR2):c.648C>T (p.Leu216=)	CCR2	Single nucleotide variant (synonymous variant)	CCR2-related disorder	GLikely benign
Select item 3059948	NM_001123396.4(CCR2):c.780T>C (p.Asn260=)	CCR2	Single nucleotide variant (synonymous variant)	CCR2-related disorder	GBenign
Select item 3052543	NM_001123396.4(CCR2):c.849G>T (p.Leu283=)	CCR2	Single nucleotide variant (synonymous variant)	CCR2-related disorder	GLikely benign
Select item 3060753	NM_001123396.4(CCR2):c.1044G>A (p.Thr348=)	CCR2	Single nucleotide variant (synonymous variant +1 more)	CCR2-related disorder	GBenign
Select item 3038731	NM_001123396.4(CCR2):c.*1189G>A	CCR2 (G355E)	Single nucleotide variant (missense variant +1 more)	CCR2-related disorder	GBenign

ClinVar