ClinVar Miner

Submissions for variant NM_000551.4(VHL):c.484del (p.Cys162fs)

dbSNP: rs1696355550
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV001310082 SCV001486209 likely pathogenic Von Hippel-Lindau syndrome no assertion criteria provided clinical testing

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