ClinVar Miner

Submissions for variant NM_014927.5(CNKSR2):c.1458A>G (p.Arg486=)

gnomAD frequency: 0.00003  dbSNP: rs760890681
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000380649 SCV000336265 uncertain significance not provided 2015-10-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000380649 SCV001068543 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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