ClinVar Miner

Submissions for variant NM_015634.4(KIFBP):c.615G>A (p.Lys205=)

gnomAD frequency: 0.00112  dbSNP: rs146627673
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000518226 SCV000613921 benign not specified 2017-03-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000904365 SCV001048879 benign not provided 2024-05-07 criteria provided, single submitter clinical testing
GeneDx RCV000904365 SCV001789971 likely benign not provided 2021-06-08 criteria provided, single submitter clinical testing

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