ClinVar Miner

Submissions for variant NM_002739.5(PRKCG):c.714C>T (p.Arg238=)

gnomAD frequency: 0.00031  dbSNP: rs367543210
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000084803 SCV000843577 benign not provided 2017-10-11 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084803 SCV000116939 not provided not provided no assertion provided not provided

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