ClinVar Miner

Submissions for variant NM_004612.4(TGFBR1):c.424A>G (p.Met142Val) (rs1029455360)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Ambry Genetics	RCV000617702	SCV000739749	uncertain significance	Cardiovascular phenotype	2018-01-16	criteria provided, single submitter	clinical testing	Insufficient evidence

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