ClinVar Miner

Submissions for variant NM_000024.5(ADRB2):c.79C>G (p.Gln27Glu) (rs1042714)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019318 SCV000039608 risk factor Asthma, childhood, susceptibility to 2005-05-01 no assertion criteria provided literature only
OMIM RCV000019319 SCV000039609 risk factor Metabolic syndrome, susceptibility to 2005-05-01 no assertion criteria provided literature only
OMIM RCV000033191 SCV000057035 benign ADRB2 POLYMORPHISM 2005-05-01 no assertion criteria provided literature only

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