ClinVar Miner

Submissions for variant NM_001244008.2(KIF1A):c.2721GGA[12] (p.Glu917dup) (rs10594016)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000593567 SCV000701115 likely benign not specified 2016-12-16 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000992250 SCV001144370 benign not provided 2018-09-28 criteria provided, single submitter clinical testing
GeneDx RCV000992250 SCV001881240 benign not provided 2015-04-22 criteria provided, single submitter clinical testing

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