ClinVar Miner

Submissions for variant NM_012309.5(SHANK2):c.207+15C>T

gnomAD frequency: 0.00908  dbSNP: rs77851214
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
Illumina Laboratory Services, Illumina RCV000315214 SCV000373877 uncertain significance Autism spectrum disorder 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693057 SCV005190432 uncertain significance not provided criteria provided, single submitter not provided

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