ClinVar Miner

Submissions for variant NM_001079668.3(NKX2-1):c.448C>G (p.Pro150Ala)

dbSNP: rs1555349335
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502603 SCV000596031 likely benign not specified 2017-11-17 criteria provided, single submitter clinical testing

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