ClinVar Miner

Submissions for variant GRCh37/hg19 2q31.2(chr2:179522225-179523982)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV002293048 SCV002585875 uncertain significance not provided 2022-09-01 criteria provided, single submitter clinical testing

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