ClinVar Miner

Submissions for variant NM_007325.5(GRIA3):c.1502G>C (p.Arg501Thr)

dbSNP: rs1556317780
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000622505 SCV000741277 likely pathogenic Inborn genetic diseases 2016-02-09 criteria provided, single submitter clinical testing

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