ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.5680C>T (p.Pro1894Ser) (rs774509236)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics,Fulgent Genetics RCV000765881 SCV000897283 uncertain significance Coffin-Siris syndrome 1 2018-10-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000194179 SCV000246535 uncertain significance not specified 2015-06-11 criteria provided, single submitter clinical testing

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