ClinVar Miner

Submissions for variant NM_001101426.4(CRPPA):c.1251+4G>A (rs753402341)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000416168 SCV000493595 uncertain significance not provided 2016-07-31 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000342731 SCV000468005 uncertain significance Congenital Muscular Dystrophy, alpha-dystroglycan related 2016-06-14 criteria provided, single submitter clinical testing

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