ClinVar Miner

Submissions for variant NM_001709.5(BDNF):c.196G>A (p.Val66Met) (rs6265)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000155463 SCV000205154 benign not specified 2013-06-18 criteria provided, single submitter clinical testing Benign with respect to pulmonary disease based on high population frequency, Th is variant has been proposed to be associated with a rnage of psychiatric manife stations though the data is not solid and more recent meta-analyses argue agains t a risk effect.
PreventionGenetics,PreventionGenetics RCV000155463 SCV000316419 benign not specified criteria provided, single submitter clinical testing
OMIM RCV000019267 SCV000039555 risk factor Memory impairment, susceptibility to 2019-09-18 no assertion criteria provided literature only

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