ClinVar Miner

Submissions for variant NM_002206.3(ITGA7):c.1008C>T (p.Asp336=) (rs145114073)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000358081 SCV000337962 likely benign not specified 2015-12-24 criteria provided, single submitter clinical testing
Invitae RCV000556411 SCV000648291 benign Muscular dystrophy, congenital, due to integrin alpha-7 deficiency 2017-12-05 criteria provided, single submitter clinical testing

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