ClinVar Miner

Submissions for variant GRCh38/hg38 18p11.32(chr18:2770295-2816145)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000141087 SCV000181953 uncertain significance See cases 2011-04-30 no assertion criteria provided clinical testing

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