ClinVar Miner

Submissions for variant GRCh38/hg38 17p13.2(chr17:3640170-3656795)x1

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 4 RCV000136977 SCV000196355 conflicting data from submitters See cases 2010-03-30 no assertion criteria provided clinical testing Uncertain significance(2), Benign (1)
ISCA site 8 RCV000136977 SCV000196356 benign See cases 2010-10-19 no assertion criteria provided clinical testing

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