"OMIM"[submitter] AND "CCR2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061928	NM_001123396.4(CCR2):c.59_60insAC (p.Thr21fs)	CCR2 (T21fs)	Insertion (frameshift variant)	Cystic disease of lung	GPathogenic
Select item 3061926	NM_001123396.4(CCR2):c.182T>G (p.Met61Arg)	CCR2 (M61R)	Single nucleotide variant (missense variant)	Cystic disease of lung	GPathogenic
Select item 8267	NM_001123396.4(CCR2):c.190G>A (p.Val64Ile)	CCR2 (V64I)	Single nucleotide variant (missense variant)	CCR2-related disorder +1 more	GBenign; protective
Select item 3061929	NM_001123396.4(CCR2):c.356T>G (p.Leu119Arg)	CCR2 (L119R)	Single nucleotide variant (missense variant)	Cystic disease of lung	GPathogenic
Select item 3061925	NM_001123396.4(CCR2):c.641_646del (p.Pro214_Leu215del)	CCR2	Deletion (inframe_deletion)	Cystic disease of lung	GPathogenic
Select item 3061927	NM_001123396.4(CCR2):c.887C>A (p.Thr296Asn)	CCR2 (T296N)	Single nucleotide variant (missense variant)	Cystic disease of lung	GPathogenic

ClinVar