ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6806A>G (p.Asn2269Ser)

gnomAD frequency: 0.00634  dbSNP: rs61729060
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000221957 SCV000269913 benign not specified 2012-04-30 criteria provided, single submitter clinical testing Asn2269Ser in Exon 21 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.6% (54/3292) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61729060).
PreventionGenetics, part of Exact Sciences RCV000221957 SCV000306118 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000905231 SCV000727305 benign not provided 2019-02-26 criteria provided, single submitter clinical testing
Invitae RCV000905231 SCV001049801 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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