ClinVar Miner

Submissions for variant GRCh37/hg19 17p12(chr17:15633426-15648509)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA Site 6 RCV000448287 SCV000500114 benign/likely benign See cases no assertion criteria provided clinical testing Likely benign (1), Benign (6)

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