ClinVar Miner

Submissions for variant NM_144508.5(KNL1):c.2311G>A (p.Val771Ile)

gnomAD frequency: 0.00107  dbSNP: rs151288115
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
Genetic Services Laboratory, University of Chicago RCV000501475 SCV000593848 uncertain significance not specified 2015-10-05 criteria provided, single submitter clinical testing
Invitae RCV000900271 SCV001044579 likely benign not provided 2018-03-30 criteria provided, single submitter clinical testing

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