ClinVar Miner

Submissions for variant NM_000551.4(VHL):c.186_187delinsTT (p.Val62_Leu63=)

dbSNP: rs2125124945
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001448658 SCV001651754 likely benign Chuvash polycythemia; Von Hippel-Lindau syndrome 2020-12-01 criteria provided, single submitter clinical testing

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