ClinVar Miner

Submissions for variant GRCh37/hg19 6q16.1(chr6:96028232-97247130)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV001251052 SCV001426455 likely pathogenic Microcephaly; Intellectual disability 2020-04-08 no assertion criteria provided clinical testing

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