ClinVar Miner

Submissions for variant NM_002206.3(ITGA7):c.1567+8C>T (rs755842392)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000359409 SCV000380250 uncertain significance Congenital Muscular Dystrophy, ITGA7-related 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000647143 SCV000768930 likely benign Muscular dystrophy, congenital, due to integrin alpha-7 deficiency 2017-09-06 criteria provided, single submitter clinical testing

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