ClinVar Miner

Submissions for variant GRCh37/hg19 Xp21.1(chrX:33183494-33640512)x2

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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 RCV000511368 SCV000586638 uncertain significance See cases 2016-03-10 no assertion criteria provided clinical testing
GenomeConnect, ClinGen RCV000509246 SCV000607119 not provided Becker muscular dystrophy; Duchenne muscular dystrophy no assertion provided phenotyping only 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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