ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.255T>G (p.Phe85Leu)

dbSNP: rs1672552627
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Constitutional Genetics Lab, Leon Berard Cancer Center RCV001250025 SCV001423950 uncertain significance Lynch-like syndrome 2019-07-01 no assertion criteria provided clinical testing

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