ClinVar Miner

Submissions for variant GRCh37/hg19 17p13.2(chr17:3543270-4045261)x3

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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 1 RCV000512393 SCV000584325 likely benign See cases 2016-02-01 no assertion criteria provided clinical testing
GenomeConnect, ClinGen RCV001249276 SCV001423222 not provided not provided no assertion provided phenotyping only Variant interpretted as Uncertain significance and reported on 04-02-2015 by Lab or GTR ID 500068. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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