ClinVar Miner

Submissions for variant NM_005359.5(SMAD4):c.905-9T>C (rs1064795175)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000484702 SCV000570721 uncertain significance not provided 2016-06-20 criteria provided, single submitter clinical testing This variant is denoted SMAD4 c.905-9T>C or IVS7-9T>C and consists of a T>C nucleotide substitution at the -9 position of intron 7 of the SMAD4 gene. This variant is not predicted to affect splicing; however, in the absence of RNA or functional studies, the actual effect of this variant is unknown. This variant has not, to our knowledge, been published in the literature as pathogenic or benign. SMAD4 c.905-9T>C was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, suggesting it is not a common benign variant in these populations. The thymine (T) nucleotide that is altered is conserved across species. Based on currently available information, it is unclear whether SMAD4 c.905-9T>C is pathogenic or benign. We consider it to be a variant of uncertain significance.
Invitae RCV000484702 SCV001066223 likely benign not provided 2018-02-05 criteria provided, single submitter clinical testing

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