ClinVar Miner

Submissions for variant GRCh38/hg38 2q13(chr2:109301667-110460985)

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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 RCV003883392 SCV004697808 uncertain significance Autism spectrum disorder no assertion criteria provided research

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