ClinVar Miner

Submissions for variant GRCh38/hg38 16p11.2(chr16:28825316-29028291)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics Department, Polish Mother's Memorial Hospital Research Institute RCV003883415 SCV004697842 pathogenic Autism spectrum disorder no assertion criteria provided research

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