ClinVar Miner

Submissions for variant NM_007144.3(PCGF2):c.194C>G (p.Pro65Arg)

dbSNP: rs1567941252
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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 RCV001727030 SCV001961681 likely pathogenic not provided 2021-07-01 criteria provided, single submitter clinical testing

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