ClinVar Miner

Submissions for variant NM_000660.7(TGFB1):c.74G>C (p.Arg25Pro) (rs1800471)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250799 SCV000305412 benign not specified criteria provided, single submitter clinical testing
GeneReviews RCV000032152 SCV000055718 benign Diaphyseal dysplasia 2015-03-05 no assertion criteria provided literature only

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