ClinVar Miner

Submissions for variant NM_000829.4(GRIA4):c.2209C>T (p.Arg737Ter)

dbSNP: rs1591461970
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dash Lab, University Health Network RCV000787968 SCV000914239 likely pathogenic Obesity 2018-05-01 no assertion criteria provided research

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