ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1616_1619del (p.Ala539fs)

dbSNP: rs2084645057
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ding PR Lab, Sun Yat-sen University Cancer Center RCV001093669 SCV001250850 likely pathogenic Lynch syndrome 1 no assertion criteria provided clinical testing

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