ClinVar Miner

Submissions for variant NM_000551.4(VHL):c.117C>G (p.Gly39=)

dbSNP: rs1057521552
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002257238 SCV002534135 likely benign Hereditary cancer-predisposing syndrome 2021-04-19 criteria provided, single submitter curation

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