ClinVar Miner

Submissions for variant NM_021956.5(GRIK2):c.808C>T (p.Arg270Ter)

dbSNP: rs1265340906
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV000790433 SCV000929760 likely pathogenic Intellectual disability 2018-03-07 criteria provided, single submitter clinical testing

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