ClinVar Miner

Submissions for variant NM_020738.4(KIDINS220):c.604-34C>T

gnomAD frequency: 0.99316  dbSNP: rs2356658
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
GeneDx RCV001614994 SCV001841972 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001614994 SCV005242038 benign not provided criteria provided, single submitter not provided

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