ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.448G>T (p.Gly150Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003148512 SCV003836419 uncertain significance Testicular anomalies with or without congenital heart disease 2022-04-18 criteria provided, single submitter clinical testing

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