ClinVar Miner

Submissions for variant NM_000579.3(CCR5):c.-301+246A>G (rs1799987)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008671 SCV000028880 pathogenic Acquired immunodeficiency syndrome, delayed progression to 2003-03-01 no assertion criteria provided literature only
OMIM RCV000008674 SCV000028883 benign CCR5 PROMOTER POLYMORPHISM 2003-07-08 no assertion criteria provided literature only
OMIM RCV000008675 SCV000028884 protective Human immunodeficiency virus type 1, susceptibility to 2003-07-08 no assertion criteria provided literature only

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