ClinVar Miner

Submissions for variant NM_000501.4(ELN):c.594G>A (p.Pro198=) (rs140337204)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000418810 SCV000535899 uncertain significance not provided 2017-01-10 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the ELN gene. The synonymous P198P (c.594 G>A) variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. It was not observed with any significant frequency in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. In addition, this substitution occurs at a nucleotide position that is conserved through mammals. Nonetheless, in silico analysis does not predict this variant will result in abnormal splicing.

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