ClinVar Miner

Submissions for variant NM_004985.5(KRAS):c.186G>A (p.Glu62=)

dbSNP: rs1407455199
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002092256 SCV002323868 likely benign RASopathy 2021-05-19 criteria provided, single submitter clinical testing

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