ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.57G>T (p.Leu19Phe)

dbSNP: rs121913538
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001354208 SCV001548761 likely pathogenic not provided no assertion criteria provided clinical testing

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