ClinVar Miner

Submissions for variant GRCh38/hg38 3p13(chr3:71518345-71562911)

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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 RCV003883416 SCV004697843 uncertain significance Autism spectrum disorder no assertion criteria provided research

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