ClinVar Miner

Submissions for variant NM_001136191.3(KANK2):c.-79-146C>T

dbSNP: rs8101045
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001713883 SCV001940010 benign not provided 2020-10-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001713883 SCV005312607 benign not provided criteria provided, single submitter not provided

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