"PreventionGenetics, part of Exact Sciences"[submitter] AND "CCR5"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8189	NM_000579.4(CCR5):c.-301+246A>G	CCR5, CCR5AS	Single nucleotide variant (intron variant)	CCR5-related condition	GBenign
Select item 3058502	NM_001394783.1(CCR5):c.69C>A (p.Ile23=)	CCR5, CCR5AS	Single nucleotide variant (synonymous variant)	CCR5-related condition	GLikely benign
Select item 2636002	NM_001394783.1(CCR5):c.74T>A (p.Val25Glu)	CCR5, CCR5AS (V25E)	Single nucleotide variant (missense variant)	CCR5-related condition	GUncertain significance
Select item 3033791	NM_001394783.1(CCR5):c.316G>A (p.Gly106Arg)	CCR5, CCR5AS (G106R)	Single nucleotide variant (missense variant)	CCR5-related condition	GLikely benign
Select item 3045114	NM_001394783.1(CCR5):c.423G>A (p.Thr141=)	CCR5, CCR5AS	Single nucleotide variant (synonymous variant)	CCR5-related condition	GLikely benign
Select item 8184	NM_001394783.1(CCR5):c.554_585del (p.Ser185fs)	CCR5, CCR5AS (S185fs)	Deletion (frameshift variant)	CCR5-related condition +1 more	GBenign
Select item 2634364	NM_001394783.1(CCR5):c.715A>G (p.Thr239Ala)	CCR5, CCR5AS (T239A)	Single nucleotide variant (missense variant)	CCR5-related condition	GUncertain significance
Select item 3057661	NM_001394783.1(CCR5):c.741C>T (p.Phe247=)	CCR5, CCR5AS	Single nucleotide variant (synonymous variant)	CCR5-related condition	GLikely benign

ClinVar