ClinVar Miner

Submissions for variant NM_015981.4(CAMK2A):c.1302C>T (p.Gly434=)

gnomAD frequency: 0.00018  dbSNP: rs376355423
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001090379 SCV001245899 likely benign not provided 2019-07-01 criteria provided, single submitter clinical testing

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