ClinVar Miner

Submissions for variant NM_015158.5(KANK1):c.2896+2T>G

dbSNP: rs149121553
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001952071 SCV002197208 uncertain significance not provided 2021-07-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479419 SCV002781669 uncertain significance Cerebral palsy, spastic quadriplegic, 2 2021-10-21 criteria provided, single submitter clinical testing

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